2-propanol has been researched along with Wilms Tumor in 105 studies
2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.
Wilms Tumor: A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The biologic peculiarities of tumors of early life are elucidated." | 2.35 | Neoplasia of early life and its relationships to teratogenesis. ( Bolande, RP, 1976) |
| "The chromosomal origin of nephroblastoma may be more frequent than estimated on the basis of its association with aniridia." | 1.27 | Del11p13/nephroblastoma without aniridia. ( Chavin-Colin, F; de Grouchy, J; Dufier, JL; Junien, C; Nihoul-Fékété, C; Turleau, C, 1984) |
| "Retinoblastoma, nephroblastoma and sympathoblastoma may be related to genome modification." | 1.27 | [Chromosome 11 and cancer]. ( Gilgenkrantz, S; Gregoire, MJ; Himont, F; Pernot, C; Pierson, M, 1983) |
| "Gene dosage effects for catalase (CAT) were studied in two unrelated patients with an interstitial deletion involving 11p13 to determine precisely the sites of the genes for CAT and the Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad (WAGR) in the 11p13 band." | 1.27 | Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306. ( Hamawaki, M; Kasai, R; Kikkawa, K; Kimira, S; Kimoto, H; Matsuoka, K; Narahara, K; Ogata, M, 1984) |
| " The chromosomic micro-deletion can be shown by using highly sophisticated cytogenetic techniques, or suspected by blood enzymatic dosage (mainly catalase)." | 1.27 | [WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases]. ( Blanc, JF; Mochon, MC; Philip, T; Plauchu, H, 1987) |
| "Bilateral nephroblastoma may be associated with congenital bilateral aniridia in children." | 1.27 | [Bilateral nephroblastoma with aniridia]. ( Alison, M; Brichon, P; Leturgeon, MC; Weyl, M, 1986) |
| "A gene dosage effect for catalase (CAT) was investigated in three individuals : one with 11p13 deletion, aniridia, ambiguous genitalla, and gonadoblastoma ; one trisomic for 11p with the exception of 11p13; and one trisomic for 11p13." | 1.26 | Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex. ( de Grouchy, J; Dufier, JL; Junien, C; Rethoré MO, L; Saïd, R; Tenconi, R; Turleau, C, 1980) |
| "The gene for red blood cell (RBC) catalase has recently been mapped to 11p13, and a gene dosage effect has been demonstrated for individuals with triplication or deletion of that region." | 1.26 | Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations. ( Ferrell, RE; Riccardi, VM, 1981) |
| "Wilms' tumor was diagnosed in two children each of whom has an identical twin." | 1.26 | The role of genetic factors in the etiology of Wilms' tumor: two pairs of monozygous twins with congenital abnormalities (aniridia; hemihypertrophy) and discordance for Wilms' tumor. ( Borges, W; Honig, GR; Maurer, HS; Pendergrass, TW, 1979) |
| " His red blood cells contained normal activities of glutathione reductase (gene on 8p) and lactate dehydrogeanse A (gene on 11p12), indicating a gene dosage consistent with the chromosomal findings." | 1.26 | Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13. ( Atkins, L; Francke, U; Holmes, LB; Riccardi, VM, 1979) |
| "The diagnosis of Wilms' tumor is usually made by excretory urography after the patient presents with an abdominal mass." | 1.25 | The incipient Wilms' tumor. ( Gay, BB; Rutherford, CR; Woodard, JR, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 103 (98.10) | 18.7374 |
| 1990's | 2 (1.90) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| MILLER, RW | 3 |
| FRAUMENI, JF | 2 |
| MANNING, MD | 1 |
| FONTANA, VJ | 1 |
| FERRARA, A | 1 |
| PERCIACCANTE, R | 1 |
| Nakagome, Y | 2 |
| Ise, T | 1 |
| Sakurai, M | 1 |
| Nakajo, T | 1 |
| Okamoto, E | 1 |
| Takano, T | 1 |
| Nakahori, Y | 1 |
| Tsuchida, Y | 1 |
| Nagahara, N | 2 |
| Takada, Y | 1 |
| Fisher, JH | 2 |
| Miller, YE | 1 |
| Sparkes, RS | 2 |
| Bateman, JB | 2 |
| Kimmel, KA | 1 |
| Carey, TE | 1 |
| Rodell, T | 1 |
| Shoemaker, SA | 2 |
| Scoggin, CH | 2 |
| Turleau, C | 3 |
| de Grouchy, J | 4 |
| Nihoul-Fékété, C | 1 |
| Dufier, JL | 2 |
| Chavin-Colin, F | 1 |
| Junien, C | 8 |
| Tournade, MF | 1 |
| Gagnadoux, MF | 1 |
| Eiferman, RA | 1 |
| Gorlin, RJ | 1 |
| Kolata, GB | 1 |
| Yunis, JJ | 2 |
| Ramsay, NK | 1 |
| Tank, ES | 1 |
| Kay, R | 1 |
| Saïd, R | 1 |
| Rethoré MO, L | 1 |
| Tenconi, R | 1 |
| Rangecroft, L | 1 |
| O'Donnell, B | 1 |
| Kousseff, BG | 1 |
| Agatucci, A | 1 |
| Hittner, HM | 3 |
| Riccardi, VM | 9 |
| Ferrell, RE | 4 |
| Strobel, RJ | 1 |
| Ledbetter, DH | 1 |
| Strong, L | 1 |
| Lebo, R | 2 |
| Rossazza, C | 1 |
| François, JH | 1 |
| Lamagnere, JP | 1 |
| Fryns, JP | 1 |
| Beirinckx, J | 1 |
| De Sutter, E | 2 |
| Derluyn, J | 1 |
| Francois, J | 4 |
| Van den Berghe, H | 1 |
| Behar, C | 1 |
| Droulle, C | 1 |
| Rose, JP | 1 |
| Munzer, M | 1 |
| Rochels, R | 1 |
| Zhordania, RV | 1 |
| Kulagina, OE | 1 |
| Bukhny, AE | 1 |
| Sotnikova, EN | 1 |
| Strong, LC | 3 |
| Fernbach, DJ | 1 |
| Verschraegen-Spae, MR | 1 |
| Shannon, RS | 1 |
| Mann, JR | 1 |
| Harper, E | 1 |
| Harnden, DG | 1 |
| Morten, JE | 1 |
| Herbert, A | 1 |
| Palmer, N | 1 |
| Evans, AE | 1 |
| Simola, KO | 3 |
| Knuutila, S | 1 |
| Kaitila, I | 1 |
| Pirkola, A | 1 |
| Pohja, P | 1 |
| Ohno, F | 1 |
| Yamano, T | 1 |
| Kataoka, K | 1 |
| Lewandowski, RC | 1 |
| De Blois, M | 1 |
| Philip, T | 2 |
| Lenoir, GM | 1 |
| Laurent, C | 1 |
| Robert, JM | 1 |
| Gregoire, MJ | 1 |
| Pernot, C | 1 |
| Himont, F | 1 |
| Pierson, M | 1 |
| Gilgenkrantz, S | 1 |
| Majumder, PP | 1 |
| Narahara, K | 1 |
| Kikkawa, K | 1 |
| Kimira, S | 1 |
| Kimoto, H | 1 |
| Ogata, M | 1 |
| Kasai, R | 1 |
| Hamawaki, M | 1 |
| Matsuoka, K | 1 |
| Sparkes, MC | 1 |
| Li, FP | 1 |
| Breslow, NE | 1 |
| Morgan, JM | 1 |
| Ghahremani, M | 1 |
| Miller, GA | 1 |
| Grundy, PE | 1 |
| Green, DM | 1 |
| Diller, LR | 1 |
| Pelletier, J | 1 |
| Huff, V | 1 |
| Bond, JV | 1 |
| Pilling, GP | 1 |
| Pendergrass, TW | 2 |
| Woodard, JR | 2 |
| Gay, BB | 1 |
| Rutherford, CR | 1 |
| Bolande, RP | 1 |
| Knudson, AG | 2 |
| Meadows, AT | 1 |
| Coucke, D | 1 |
| Coppieters, R | 1 |
| Dutau, G | 1 |
| Vaysse, P | 1 |
| Ribot, C | 1 |
| Carton, M | 1 |
| Juskiewenski, S | 1 |
| Rochiccioli, P | 1 |
| Dolota, W | 1 |
| Ordyniec, J | 1 |
| Sujansky, E | 1 |
| Smith, AC | 1 |
| Francke, U | 3 |
| Cotlier, E | 1 |
| Rose, M | 1 |
| Moel, SA | 1 |
| Andersen, SR | 1 |
| Geertinger, P | 1 |
| Larsen, HW | 1 |
| Mikkelsen, M | 1 |
| Vestermark, S | 1 |
| Warburg, M | 1 |
| Borges, W | 2 |
| Maurer, HS | 1 |
| Honig, GR | 1 |
| Ruprecht, KW | 1 |
| Naumann, GO | 1 |
| Holmes, LB | 1 |
| Atkins, L | 2 |
| McBride, G | 1 |
| Couillin, P | 4 |
| Azoulay, M | 2 |
| Metezeau, P | 1 |
| Grisard, MC | 1 |
| Gessler, M | 3 |
| Thomas, GH | 2 |
| McGillivray, BC | 1 |
| Hayden, M | 1 |
| Jaschek, G | 1 |
| Bruns, GA | 3 |
| Cowell, JK | 1 |
| Wadey, RB | 1 |
| Buckle, BB | 1 |
| Pritchard, J | 1 |
| Harnois, C | 1 |
| Boisjoly, HM | 1 |
| Jotterand, V | 1 |
| Boyd, PA | 3 |
| Christie, S | 2 |
| Hastie, ND | 3 |
| Porteous, DJ | 5 |
| Lavedan, C | 1 |
| Barichard, F | 1 |
| Molina Gomez, D | 1 |
| Nicolas, H | 1 |
| Quack, B | 1 |
| Rethoré, MO | 1 |
| Noel, B | 2 |
| Mochon, MC | 1 |
| Blanc, JF | 1 |
| Plauchu, H | 1 |
| Seawright, A | 3 |
| Fletcher, JM | 3 |
| Fantes, JA | 2 |
| Morrison, H | 1 |
| Li, SS | 1 |
| Van Heyningen, V | 3 |
| Hotta, Y | 1 |
| Fujiki, K | 1 |
| Ishida, N | 1 |
| Kato, K | 1 |
| Nakajima, A | 1 |
| Takamatsu, H | 1 |
| de Chadarévian, JP | 1 |
| Kaplan, P | 1 |
| Vekemans, M | 1 |
| Kaplan, BS | 1 |
| Vadot, E | 1 |
| Vercherat, M | 1 |
| Davis, LM | 2 |
| Stallard, R | 1 |
| Nowak, NJ | 2 |
| Shows, TB | 2 |
| Bickmore, W | 2 |
| Maule, J | 1 |
| Compton, DA | 1 |
| Weil, MM | 1 |
| Jones, C | 1 |
| Saunders, GF | 1 |
| Schinzel, A | 1 |
| Byers, MG | 1 |
| Fukushima, Y | 1 |
| Qin, SZ | 1 |
| Scoggin, C | 1 |
| van Kessel, AG | 1 |
| Nusse, R | 1 |
| Slater, R | 1 |
| Tetteroo, P | 1 |
| Hagemeijer, A | 1 |
| Barletta, C | 1 |
| Castello, MA | 1 |
| Ferrante, E | 1 |
| Mavelli, I | 1 |
| Clerico, A | 1 |
| Ciriolo, MR | 1 |
| Vignetti, P | 1 |
| Michalopoulos, EE | 1 |
| Bevilacqua, PJ | 1 |
| Stokoe, N | 1 |
| Powers, VE | 1 |
| Willard, HF | 1 |
| Lewis, WH | 1 |
| Morse, H | 1 |
| Leigh, T | 1 |
| Buckton, KE | 1 |
| Spowart, G | 1 |
| Hill, RE | 1 |
| Newton, MS | 1 |
| Weyl, M | 1 |
| Brichon, P | 1 |
| Leturgeon, MC | 1 |
| Alison, M | 1 |
| Schmickel, RD | 1 |
| Trigg, ME | 1 |
| Padilla-Nash, H | 1 |
| Saxe, D | 1 |
| Friedman, A | 1 |
| Uehling, D | 1 |
| France, T | 1 |
| Gilbert, E | 1 |
| Wilms, H | 1 |
| Back, E | 1 |
| Kirste, G | 1 |
| Mannens, M | 1 |
| Slater, RM | 1 |
| Heyting, C | 1 |
| Geurts van Kessel, A | 1 |
| Goedde-Salz, E | 1 |
| Frants, RR | 1 |
| Van Ommen, GJ | 1 |
| Pearson, PL | 1 |
| Howell, RT | 1 |
| Gardner, A | 1 |
| Dickinson, V | 1 |
| Cranston, G | 1 |
| Gosden, JR | 1 |
| Rout, D | 1 |
| Ogura, A | 1 |
| Kamei, Y | 1 |
| Fujita, Y | 1 |
| DiGeorge, AM | 3 |
| Harley, RD | 2 |
| Glass, AG | 1 |
| Mackintosh, TF | 1 |
| Girdwood, TG | 1 |
| Parker, DJ | 1 |
| Strachan, IM | 1 |
| Campinchi, R | 2 |
| Schweisguth, C | 1 |
| Lemerle, P | 1 |
| Pivoteau, P | 1 |
| Levine, MK | 1 |
| Flanagan, JC | 1 |
| Fauré, C | 1 |
| Lange, JC | 1 |
| Schweisguth, O | 1 |
| Pivoteau, B | 1 |
| Lemerle, J | 1 |
| Gandhi, RK | 1 |
| Deshmukh, SS | 1 |
| Waingankar, VS | 1 |
| Evans, DI | 1 |
| Holzel, A | 1 |
| De Andres Basauri, L | 1 |
| Martínez, C | 1 |
| Ladda, R | 1 |
| Littlefield, J | 1 |
| Neurath, P | 1 |
| Marimuthu, KM | 1 |
| Neidhardt, M | 1 |
6 reviews available for 2-propanol and Wilms Tumor
| Article | Year |
|---|---|
Recent advances in cytogenetics.
Topics: Chromosome Banding; Chromosome Deletion; Chromosome Fragility; Cytogenetics; DiGeorge Syndrome; Flow | 1983 |
High-resolution cytogenetics.
Topics: Adolescent; Chromosome Aberrations; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, 13- | 1983 |
Neoplasia of early life and its relationships to teratogenesis.
Topics: Abnormalities, Drug-Induced; Carcinoma, Basal Cell; Chromosome Aberrations; Chromosome Disorders; Co | 1976 |
[Newly discovered structural chromosome aberrations in long familial syndromes, associations and sequences. Prader-Willi syndrome, Miller-Dieker syndrome, Giedion-Langer syndrome, Aniridia-Wilms' tumor association, DiGeorge sequence, Wiedemann-Beckwith sy
Topics: Abnormalities, Multiple; Brain; Child; Chromosome Aberrations; Chromosome Disorders; DiGeorge Syndro | 1988 |
Contiguous gene syndromes: a component of recognizable syndromes.
Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping | 1986 |
[Wilms' tumor and congenital malformations].
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Di | 1973 |
99 other studies available for 2-propanol and Wilms Tumor
| Article | Year |
|---|---|
ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS.
Topics: Adolescent; Aniridia; Child; Congenital Abnormalities; Cryptorchidism; Hemangioma; Humans; Hyperplas | 1964 |
WILMS'S TUMOR AND ASSOCIATED ANOMALIES.
Topics: Cataract; Child; Congenital Abnormalities; Ear Deformities, Acquired; Ear, External; Humans; Iris; N | 1965 |
High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities.
Topics: Adolescent; Child; Child, Preschool; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, 6- | 1984 |
Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene.
Topics: Animals; Antigens, Surface; Cell Line; Child, Preschool; Chromosome Deletion; Chromosomes, Human, 6- | 1984 |
Del11p13/nephroblastoma without aniridia.
Topics: Acatalasia; Catalase; Child, Preschool; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, | 1984 |
Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature.
Topics: Acatalasia; Adolescent; Child, Preschool; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Femal | 1984 |
Association of Wilms' tumor with Peter's anomaly.
Topics: Cataract; Corneal Opacity; Humans; Infant; Infant, Newborn; Iris; Kidney Neoplasms; Male; Syndrome; | 1984 |
Genes and cancer: the story of Wilms tumor.
Topics: Age Factors; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, | 1980 |
Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
Topics: Abnormalities, Multiple; Adolescent; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; | 1980 |
Birth defects and cancer due to small chromosomal deletions.
Topics: Chromosome Deletion; Chromosomes, Human, 6-12 and X; Humans; Iris; Kidney Neoplasms; Syndrome; Wilms | 1980 |
Neoplasms associated with hemihypertophy, Beckwith-Wiedemann syndrome and aniridia.
Topics: Abnormalities, Multiple; Adrenal Cortex Neoplasms; Child, Preschool; Female; Fetal Growth Retardatio | 1980 |
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.
Topics: Adolescent; Catalase; Child; Chromosome Mapping; Chromosomes, Human, 6-12 and X; Clinical Enzyme Tes | 1980 |
Wilms' tumour and associated congenital anomalies.
Topics: Child, Preschool; Face; Female; Humans; Infant; Iris; Kidney Neoplasms; Male; Wilms Tumor | 1980 |
Aniridia-Wilms tumor association.
Topics: Adolescent; Female; Humans; Iris; Iris Diseases; Kidney Neoplasms; Male; Wilms Tumor | 1981 |
Genetic heterogeneity of aniridia: negative linkage data.
Topics: Acid Phosphatase; Female; Genetic Linkage; Humans; Infant; Iris; L-Lactate Dehydrogenase; Male; Wilm | 1980 |
[Aniridia and nephroblastoma].
Topics: Cataract; Child, Preschool; Humans; Infant; Infant, Newborn; Iris; Kidney Neoplasms; Male; Wilms Tum | 1980 |
Aniridia-Wilms' tumor association and 11p interstitial deletion.
Topics: Child, Preschool; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Humans; Intellectual Disabili | 1981 |
[A new case of association of aniridia and nephroblastoma in a hemophilic child].
Topics: Antineoplastic Agents; Child, Preschool; Hemophilia A; Humans; Iris; Kidney Neoplasms; Male; Wilms T | 1980 |
[Aniridia and Wilms' tumor (Miller's syndrome)].
Topics: Humans; Iris; Kidney Neoplasms; Syndrome; Wilms Tumor | 1981 |
[Combination of nephroblastoma and aniridia in a child with congenital deletion of chromosome 11].
Topics: Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Humans; Iris; K | 1981 |
Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations.
Topics: Catalase; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Erythrocytes; Female; Genes, Dominant | 1981 |
Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes.
Topics: Adolescent; Chromosome Deletion; Chromosomes, Human, 13-15; Chromosomes, Human, 6-12 and X; Female; | 1982 |
[Aniridia and Wilm's tumor].
Topics: Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 6-12 and X; Female; Humans; Infant, Ne | 1981 |
Wilms's tumour and aniridia: clinical and cytogenetic features.
Topics: Child, Preschool; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Female; Humans; Infant; Iris; | 1982 |
The significance of genetic research in ophthalmology.
Topics: Chromosome Deletion; Chromosomes, Human, 6-12 and X; Eye Diseases; Eye Neoplasms; Fabry Disease; Hum | 1982 |
Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
Topics: Abnormalities, Multiple; Chromosome Deletion; Chromosomes, Human, 13-15; Eye Neoplasms; Female; Huma | 1982 |
The association of aniridia and Wilms' tumor: methods of surveillance and diagnosis.
Topics: Child, Preschool; Humans; Infant; Iris; Kidney Neoplasms; Male; Risk; Urography; Wilms Tumor | 1983 |
Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor.
Topics: Chromosome Banding; Female; Humans; Infant, Newborn; Iris; Karyotyping; Kidney Neoplasms; Male; Pedi | 1983 |
A case of congenital aniridia and familial pheochromocytoma--with special reference to aniridia-Wilms' tumor syndrome.
Topics: Adolescent; Adrenal Gland Neoplasms; Female; Humans; Iris; Kidney Neoplasms; Pheochromocytoma; Wilms | 1982 |
[Prometaphase cytogenetic study of 13 cases of Wilms' tumor without aniridia].
Topics: Catalase; Child; Child, Preschool; Chromosome Aberrations; Humans; Infant; Iris; Karyotyping; Kidney | 1983 |
[Chromosome 11 and cancer].
Topics: Abnormalities, Multiple; Adrenal Gland Neoplasms; Chromosome Aberrations; Chromosome Deletion; Chrom | 1983 |
Application of isozymes to the mapping of inherited ophthalmic disorders.
Topics: Acid Phosphatase; Clinical Enzyme Tests; Eye Diseases; Genes, Dominant; Gonadal Dysgenesis; Humans; | 1983 |
Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.
Topics: Abnormalities, Multiple; Adolescent; Catalase; Child, Preschool; Chromosome Banding; Chromosome Dele | 1984 |
Aniridia: enzyme studies in an 11p--chromosomal deletion.
Topics: Catalase; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, 6-1 | 1984 |
Germline WT1 mutations in Wilms' tumor patients: preliminary results.
Topics: Base Sequence; Exons; Genes, Wilms Tumor; Humans; Iris; Kidney Neoplasms; Mutation; Neoplasms, Multi | 1996 |
Genotype/phenotype correlations in Wilms' tumor.
Topics: Alleles; Amino Acid Sequence; Antisense Elements (Genetics); Child; Consensus Sequence; DNA Transpos | 1996 |
Bilateral Wilms' tumour. Age at diagnosis, associated congenital anormalies, and possible pattern of inheritance.
Topics: Age Factors; Child, Preschool; Cryptorchidism; Female; Humans; Hypospadias; Infant; Iris; Kidney; Ki | 1975 |
Wilms' tumor in seven children with congenital aniridia.
Topics: Abnormalities, Multiple; Child, Preschool; Diagnosis, Differential; Humans; Infant; Infant, Newborn; | 1975 |
Congenital anomalies in children with Wilms' tumor: a new survey.
Topics: Child; Child, Preschool; Congenital Abnormalities; Female; Genitalia; Growth Disorders; Humans; Infa | 1976 |
The incipient Wilms' tumor.
Topics: Female; Humans; Hypertrophy; Infant; Iris; Kidney Neoplasms; Urography; Wilms Tumor | 1975 |
Developmental genetics of neuroblastoma.
Topics: Carcinoma in Situ; Child; Child, Preschool; Congenital Abnormalities; Demography; Female; Ganglia, A | 1976 |
Aniridia-Wilms' tumour syndrome.
Topics: Child, Preschool; Female; Humans; Infant; Iris; Syndrome; Wilms Tumor | 1977 |
[The aniridia-nephroblastoma syndrome].
Topics: Child, Preschool; Chromosomes; Humans; Iris; Karyotyping; Kidney Neoplasms; Male; Syndrome; Wilms Tu | 1976 |
[Wilm's tumor coexisting with congenital bilateral absence of iris].
Topics: Abnormalities, Multiple; Child, Preschool; Humans; Infant; Iris; Kidney Neoplasms; Male; Wilms Tumor | 1977 |
Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
Topics: Adolescent; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Congenital | 1978 |
Aniridia, cataracts, and Wilms' tumor in monozygous twins.
Topics: Adolescent; Adult; Cataract; Child; Child, Preschool; Diabetes Mellitus; Female; Glaucoma; Humans; I | 1978 |
[P 11 deletion syndrome. Aniridia, urogenital malformation and mental retardation].
Topics: Chromosome Deletion; Chromosomes, Human, 6-12 and X; Diagnosis, Differential; Dysgerminoma; Genitali | 1978 |
Aniridia, cataracts, and Wilms tumor.
Topics: Cataract; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Female; Huma | 1978 |
The role of genetic factors in the etiology of Wilms' tumor: two pairs of monozygous twins with congenital abnormalities (aniridia; hemihypertrophy) and discordance for Wilms' tumor.
Topics: Abnormalities, Multiple; Child, Preschool; Diseases in Twins; Female; Humans; Hypertrophy; Infant; I | 1979 |
[Aniridia and Wilm's tumor].
Topics: Child; Child, Preschool; Female; Humans; Infant; Iris; Kidney Neoplasms; Male; Syndrome; Wilms Tumor | 1978 |
Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.
Topics: Abnormalities, Multiple; Child; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, 6-12 an | 1979 |
Chromosome analysis techniques expand; new links to cancer.
Topics: Child; Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosomes, Human, 13-15; | 1979 |
Aniridia caused by a heritable chromosome 11 deletion.
Topics: Abnormalities, Multiple; Cataract; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Female; Geni | 1979 |
The gene for catalase is assigned between the antigen loci MIC4 and MIC11.
Topics: Antigens; Catalase; Child; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; Fem | 1989 |
A deletion map of the WAGR region on chromosome 11.
Topics: Abnormalities, Multiple; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA P | 1989 |
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.
Topics: Cell Line; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA; Humans; Hybrid | 1989 |
Sporadic aniridia and Wilms' tumor: visual function evaluation of three cases.
Topics: Chromosome Deletion; Chromosomes, Human, Pair 11; Contact Lenses; Electroretinography; Evoked Potent | 1989 |
Cloning of breakpoints of a chromosome translocation identifies the AN2 locus.
Topics: Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 4; Cl | 1989 |
Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11.
Topics: Chromosome Mapping; Chromosomes, Human, Pair 11; DNA; Genetic Markers; Humans; Iris; Kidney Neoplasm | 1989 |
Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.
Topics: Adult; Blotting, Southern; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Ch | 1989 |
[WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases].
Topics: Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosomes, Human, Pair 11; Disor | 1987 |
Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
Topics: Animals; Cell Separation; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 11; DNA; | 1988 |
High resolution G-banding analysis in aniridia.
Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Female; Humans; | 1987 |
Aniridia/glaucoma and Wilms tumor in a sibship with renal tubular acidosis and sensory nerve deafness.
Topics: Acidosis, Renal Tubular; Adult; Consanguinity; Deafness; Diabetes Mellitus, Type 1; Genes, Recessive | 1987 |
[The aniridia-Wilms' tumor syndrome: a familial case].
Topics: Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 11; Female; Humans; Infant; Iris; Ki | 1987 |
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
Topics: Animals; Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 11; DNA; Humans; Hybrid Cells; Iri | 1988 |
Molecular analysis of the aniridia--Wilms' tumor syndrome.
Topics: Chromosome Mapping; Chromosomes, Human, Pair 11; Genetic Markers; Humans; Iris; Kidney Neoplasms; Sy | 1988 |
Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.
Topics: Chromosome Mapping; Chromosomes, Human, Pair 11; DNA Probes; Electrophoresis, Agar Gel; Genetic Link | 1988 |
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
Topics: Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 11; Cloning, Molecular; DNA; Electrophoresi | 1988 |
Four new DNA markers are assigned to the WAGR region of 11p13: isolation and regional assignment of 112 chromosome 11 anonymous DNA segments.
Topics: Catalase; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; Cloning, Molecular; | 1988 |
Localization of the oncogene c-Ha-ras1 outside the aniridia-Wilms' tumor-associated deletion of chromosome 11(del 11p13) using somatic cell hybrids.
Topics: Chromosome Deletion; Chromosomes, Human, 6-12 and X; Congenital Abnormalities; Humans; Iris; Male; O | 1985 |
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 17-1985. A 13-year-old boy with aniridia and proteinuria 11 years after nephrectomy for a Wilms' tumor.
Topics: Adolescent; Basement Membrane; Glomerular Mesangium; Glomerulonephritis; Glomerulosclerosis, Focal S | 1985 |
11p13 deletion and reduced RBC catalase in a patient with aniridia, glaucoma and bilateral Wilms' tumor.
Topics: Catalase; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Erythrocytes; Glaucoma; Humans; Infan | 1985 |
Molecular analysis of gene deletion in aniridia--Wilms tumor association.
Topics: Animals; Catalase; Cell Line; Chromosome Banding; Chromosome Deletion; Chromosome Mapping; Chromosom | 1985 |
High-resolution studies in patients with aniridia-Wilms tumor association.
Topics: Chromosome Aberrations; Chromosomes, Human, 6-12 and X; Female; Humans; Iris; Male; Wilms Tumor | 1985 |
The E7-associated cell-surface antigen: a marker for the 11p13 chromosomal deletion associated with aniridia-Wilms tumor.
Topics: Abnormalities, Multiple; Animals; Antibodies, Monoclonal; Antigens, Surface; Child; Chromosome Bandi | 1985 |
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
Topics: Antigens, Surface; Calcitonin; Catalase; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human | 1985 |
[Bilateral nephroblastoma with aniridia].
Topics: Chromosome Deletion; Chromosomes, Human, 6-12 and X; Humans; Infant; Iris; Kidney Neoplasms; Male; O | 1986 |
Aniridia and Wilms' tumor in a child constitutionally mosaic for 11p-;12q+: a new chromosomal change also present in Wilms' tumor cells of the blastema type.
Topics: Cells; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Female; Humans; Infant; Iris; Kidney Neo | 1986 |
[Terminal renal failure in aniridia-Wilms syndrome].
Topics: Adult; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 1 | 1986 |
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions.
Topics: Animals; Chromosome Banding; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; C | 1987 |
G and R banding of 11p deletions in aniridia--Wilms' tumour.
Topics: Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 11; Humans; Infant; Iris; Wilms Tu | 1987 |
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
Topics: Animals; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 11; Cloning, Molecular; D | 1987 |
[A case of aniridia-Wilms' tumor syndrome].
Topics: Chromosome Deletion; Chromosomes, Human, Pair 11; Female; Humans; Infant; Iris; Kidney Neoplasms; Sy | 1987 |
The association of aniridia, Wilms's tumor, and genital abnormalities.
Topics: Cataract; Child, Preschool; Disorders of Sex Development; Humans; Iris; Male; Wilms Tumor | 1965 |
The association of aniridia, Wilms' tumor, and genital abnormalities.
Topics: Child, Preschool; Female; Humans; Infant; Iris; Male; Urogenital Abnormalities; Wilms Tumor | 1966 |
Wilms' tumor and congenital aniridia.
Topics: Abnormalities, Multiple; Child; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Iris; Mal | 1968 |
Aniridia and wilms's tumour (nephroblastoma).
Topics: Bronchopneumonia; Child, Preschool; Eye Diseases; Female; Humans; Iris; Kidney Neoplasms; Wilms Tumo | 1968 |
[Associated aniridia and nephroblastoma].
Topics: Child, Preschool; Female; Humans; Infant; Iris; Kidney Neoplasms; Wilms Tumor | 1968 |
Nephroblastoma (Wilms tumor) and congenital aniridia.
Topics: Female; Humans; Infant; Iris; Kidney; Nephrectomy; Nystagmus, Pathologic; Urography; Wilms Tumor | 1969 |
Sporadic aniridia and Wilms' tumor.
Topics: Adult; Age Factors; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Infant; Iris; Kidney | 1969 |
[Nephroblastoma and aniridia].
Topics: Female; Humans; Infant; Iris; Kidney Neoplasms; Wilms Tumor | 1967 |
Childhood cancer and congenital defects. A study of U.S. death certificates during the period 1960-1966.
Topics: Adolescent; Bone and Bones; Brain; Congenital Abnormalities; Craniofacial Dysostosis; Cystic Fibrosi | 1969 |
[The association of aniridia with tumor of the kidney in children. 4 cases].
Topics: Child, Preschool; Eye Diseases; Female; Humans; Infant; Iris; Kidney Neoplasms; Microcephaly; Nystag | 1967 |
Wilm's tumor with aniridia.
Topics: Child, Preschool; Humans; Iris; Male; Wilms Tumor | 1970 |
Mutation and cancer: a model for Wilms' tumor of the kidney.
Topics: Child, Preschool; Chromosomes; Diseases in Twins; Eye Neoplasms; Factor Analysis, Statistical; Femal | 1972 |
Wilm's-aniridia syndrome with transient hypo-gamma-globulinaemia of infancy.
Topics: Agammaglobulinemia; Cataract; Child, Preschool; Diet Therapy; Ear, External; Eczema; Hematuria; Huma | 1973 |
Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome.
Topics: Abnormalities, Multiple; Cataract; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; C | 1974 |
[Wilms' tumor and aniridia--a genetically determined syndrome?].
Topics: Abnormalities, Multiple; Cryptorchidism; Humans; Infant; Intellectual Disability; Iris; Kidney Neopl | 1972 |