2-propanol has been researched along with Autosomal Chromosome Disorders in 75 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.
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) |
"Karotype studies showed several chromosomal abnormalities following radiotherapy." | 1.27 | Fibroblast radiosensitivity and intraocular fibrovascular proliferation following radiotherapy for bilateral retinoblastoma. ( Albert, DM; Cassady, JR; Leombruno, D; Little, JB; Puliafito, CA; Trantravahi, R; Walton, DS; Weichselbaum, RR, 1986) |
" 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) |
"The maculas showed subretinal hemorrhages, glial cicatrization of the outer retinal layers, and profound choroidal atrophy, particularly in the advanced stages of the disease." | 1.26 | Pseudoinflammatory fundus dystrophy with autosomal recessive inheritance. ( Alanko, HI; Eriksson, AW; Forsius, HR; Suvanto, EA, 1982) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 64 (85.33) | 18.7374 |
1990's | 9 (12.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (2.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Shah, S | 1 |
Koban, Y | 1 |
Le, BHA | 1 |
Bechtold, M | 1 |
Zolfaghari, E | 1 |
Kim, JW | 1 |
Berry, JL | 1 |
Morrison, PJ | 1 |
COGAN, DG | 1 |
KUWABARA, T | 1 |
LELE, KP | 1 |
DENT, T | 1 |
DELHANTY, JD | 1 |
Edwards, JH | 1 |
Yuncken, C | 1 |
Rushton, DI | 1 |
Richards, S | 1 |
Mittwoch, U | 1 |
Leão, JC | 1 |
Bargman, GJ | 1 |
Neu, RL | 1 |
Kajii, T | 2 |
Gardner, LI | 1 |
Petit, P | 1 |
Godart, S | 1 |
Fryns, JP | 3 |
Kolata, GB | 1 |
Yunis, JJ | 1 |
Ramsay, NK | 1 |
Zhordania, RV | 1 |
Kulagina, OE | 1 |
Bukhny, AE | 1 |
Sotnikova, EN | 1 |
Bateman, JB | 1 |
Sparkes, MC | 1 |
Sparkes, RS | 1 |
Ferry, AP | 1 |
Marchevsky, A | 1 |
Strauss, L | 1 |
Torczynski, E | 1 |
Calderone, JP | 1 |
Chess, J | 1 |
Borodic, G | 1 |
Albert, DM | 3 |
Ferrell, RE | 2 |
Chakravarti, A | 1 |
Hittner, HM | 2 |
Riccardi, VM | 3 |
Schanzlin, DJ | 1 |
Goldberg, DB | 1 |
Brown, SI | 1 |
Clark, CE | 1 |
Telfer, MA | 1 |
Cowell, HR | 1 |
Kalamchi, A | 1 |
Steg, NL | 1 |
Niikawa, N | 1 |
Fukushima, Y | 1 |
Taniguchi, N | 1 |
Iizuka, S | 1 |
Forsius, HR | 1 |
Eriksson, AW | 1 |
Suvanto, EA | 1 |
Alanko, HI | 1 |
Cebon, L | 1 |
West, RH | 1 |
Borda, RR | 1 |
Justice, J | 1 |
Warburg, M | 1 |
Mikkelsen, M | 1 |
Andersen, SR | 1 |
Geertinger, P | 1 |
Larsen, HW | 1 |
Vestermark, S | 1 |
Parving, A | 1 |
Fledelius, HC | 1 |
Nicolosi, C | 1 |
Girlanda, P | 1 |
Vita, G | 1 |
Messina, C | 1 |
Bulle, F | 1 |
Lespinasse, J | 1 |
Pawlak, A | 1 |
Vadot, E | 1 |
Sastre, J | 1 |
Noël, B | 3 |
Guellaen, G | 1 |
Ramesh, KH | 1 |
Shah, HO | 1 |
Sherman, J | 1 |
Lin, JH | 1 |
Verma, RS | 1 |
Monaghan, KG | 1 |
Van Dyke, DL | 1 |
Wiktor, A | 1 |
Feldman, GL | 1 |
Dollfus, H | 1 |
Joanny-Flinois, O | 1 |
Doco-Fenzy, M | 1 |
Veyre, L | 1 |
Joanny-Flinois, L | 1 |
Khoury, M | 1 |
Jonveaux, P | 1 |
Abitbol, M | 1 |
Dufier, JL | 1 |
Mills, MD | 1 |
Syed, N | 1 |
Bolande, RP | 1 |
Borges, W | 1 |
McBride, G | 1 |
Walknowska, J | 1 |
Peakman, D | 1 |
Weleber, RG | 1 |
Fulton, AB | 1 |
Howard, RO | 1 |
Hsia, YE | 1 |
Packman, S | 1 |
Bartsch, O | 1 |
Aksu, F | 1 |
Fenner, A | 1 |
Schwinger, E | 1 |
Pallotta, R | 1 |
Walton, DS | 1 |
Weichselbaum, RR | 1 |
Cassady, JR | 1 |
Little, JB | 1 |
Leombruno, D | 1 |
Trantravahi, R | 1 |
Puliafito, CA | 1 |
Lavedan, C | 1 |
Barichard, F | 1 |
Azoulay, M | 1 |
Couillin, P | 1 |
Molina Gomez, D | 1 |
Nicolas, H | 1 |
Quack, B | 2 |
Rethoré, MO | 1 |
Junien, C | 1 |
Ward, J | 1 |
Sierra, IA | 1 |
D'Croz, E | 1 |
Mochon, MC | 1 |
Blanc, JF | 1 |
Plauchu, H | 1 |
Philip, T | 1 |
Hotta, Y | 1 |
Fujiki, K | 1 |
Ishida, N | 1 |
Kato, K | 1 |
Nakajima, A | 1 |
Takamatsu, H | 1 |
Schinzel, A | 1 |
Schmickel, RD | 1 |
Wilms, H | 1 |
Back, E | 1 |
Kirste, G | 1 |
Kleczkowska, A | 1 |
Igodt-Ameye, L | 1 |
Van den Berghe, H | 2 |
Pearce, WG | 1 |
Cory, CC | 1 |
Jamison, DL | 1 |
Lur'e, IV | 2 |
Gushchina, GS | 1 |
Rogers, GL | 1 |
Polomeno, RC | 1 |
De Andres Basauri, L | 1 |
Martínez, C | 1 |
Ladda, R | 1 |
Atkins, L | 1 |
Littlefield, J | 1 |
Neurath, P | 1 |
Marimuthu, KM | 1 |
Casey, TA | 1 |
Gibbs, D | 1 |
Jerndal, T | 1 |
Mollica, F | 1 |
Pavone, L | 1 |
Antener, I | 1 |
Freedom, RM | 1 |
Gerald, PS | 1 |
Mottet, J | 1 |
Nantois, Y | 1 |
Tabbara, KF | 1 |
Khouri, FP | 1 |
Neuhäuser, G | 1 |
Timmerman, GJ | 1 |
van Olphen, AH | 1 |
Bergsma, DR | 1 |
Kaiser-Kupfer, M | 1 |
Balci, S | 1 |
Halicioglu, C | 1 |
Say, B | 1 |
Taysi, K | 1 |
Heimann, K | 1 |
Jaeger, W | 1 |
Dollmann, A | 1 |
Nagy, M | 1 |
Fazekas, A | 1 |
Cordier, J | 1 |
Reny, A | 1 |
Kahn, N | 1 |
Eggermont, E | 1 |
Veresen, H | 1 |
Darby, CW | 1 |
Hughes, DT | 1 |
Dallapiccola, B | 1 |
Fraser, GR | 1 |
Klein, D | 1 |
Flickinger, RR | 1 |
Spivey, BE | 1 |
François, J | 1 |
Hanssens, M | 1 |
Arias, D | 1 |
Passarge, E | 1 |
Engle, MA | 1 |
German, J | 1 |
Cagianut, B | 1 |
Theiler, K | 1 |
Holland, MG | 1 |
Cambie, E | 1 |
10 reviews available for 2-propanol and Autosomal Chromosome Disorders
Article | Year |
---|---|
The iris - a window into the genetics of common and rare eye diseases.
Topics: Chromosome Disorders; Cornea; Eye Diseases; Humans; Iris; Iris Diseases | 2010 |
Normal and abnormal ocular development in man.
Topics: Chromosome Aberrations; Chromosome Disorders; Coloboma; Corneal Ulcer; Ectoderm; Eye; Eye Abnormalit | 1982 |
Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.
Topics: Abnormalities, Multiple; Autistic Disorder; Cataract; Child, Preschool; Chromosome Aberrations; Chro | 1997 |
Neoplasia of early life and its relationships to teratogenesis.
Topics: Abnormalities, Drug-Induced; Carcinoma, Basal Cell; Chromosome Aberrations; Chromosome Disorders; Co | 1976 |
Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.
Topics: Abnormalities, Multiple; Blepharoptosis; Child; Chromosome Aberrations; Chromosome Disorders; Chromo | 1991 |
[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 |
[Eye anomalies in chromosomal aberrations].
Topics: Abnormalities, Multiple; Aneuploidy; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Huma | 1971 |
[Wilms' tumor and congenital malformations].
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Di | 1973 |
[Ocular signs of trisomy 13. General review].
Topics: Anterior Chamber; Brain; Cataract; Child; Child, Preschool; Choroid; Chromosome Aberrations; Chromos | 1971 |
65 other studies available for 2-propanol and Autosomal Chromosome Disorders
Article | Year |
---|---|
Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion.
Topics: Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 13; Diagnosis, Differential; DNA | 2018 |
OCULAR PATHOLOGY OF THE 13-15 TRISOMY SYNDROME.
Topics: Cartilage; Cataract; Chromosome Disorders; Chromosomes, Human, Pair 13; Humans; Infant; Iris; Ophtha | 1964 |
CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS.
Topics: Biopsy; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Coloboma; Congenital Abnor | 1965 |
Three cases of triploidy in man.
Topics: Abortion, Spontaneous; Blood Group Antigens; Cell Nucleus; Chromosome Aberrations; Chromosome Disord | 1967 |
New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.
Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 4-5; Cri-du-Chat | 1967 |
Silver staining of the supernumerary chromosome in the cat-eye syndrome.
Topics: Anus, Imperforate; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; C | 1980 |
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 |
[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 |
Aniridia: enzyme studies in an 11p--chromosomal deletion.
Topics: Catalase; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, 6-1 | 1984 |
Ocular abnormalities in deletion of the long arm of chromosome 11.
Topics: Choroid; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, 6-12 | 1981 |
Intraocular pathology of trisomy 18 (Edwards's syndrome): report of a case and review of the literature.
Topics: Anterior Chamber; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Eye; Fema | 1983 |
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2.
Topics: Acid Phosphatase; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Hu | 1980 |
Hallermann-Streiff syndrome associated with sclerocornea, aniridia, and a chromosomal abnormality.
Topics: Adult; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and | 1980 |
Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
Topics: Abnormalities, Multiple; Adult; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13 | 1982 |
Chromosome abnormalities involving 11p13 and low erythrocyte catalase activity.
Topics: Catalase; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chrom | 1982 |
Pseudoinflammatory fundus dystrophy with autosomal recessive inheritance.
Topics: Adult; Chromosome Aberrations; Chromosome Disorders; Consanguinity; Diagnosis, Differential; Female; | 1982 |
A syndrome involving congenital cataracts of unusual morphology, microcornea, abnormal irides, nystagmus and congenital glaucoma, inherited as an autosomal dominant trait.
Topics: Adult; Aged; Cataract; Child; Chromosome Aberrations; Chromosome Disorders; Cornea; Diagnosis, Diffe | 1982 |
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Elec | 1980 |
Aniridia and interstitial deletion of the short arm of chromosome 11.
Topics: Cataract; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Dysgerminoma | 1980 |
Ultrasonic evaluation of microphthalmos and coloboma. A discussion of 3 cases, with emphasis on microphthalmos with orbital cyst.
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 13; | 1996 |
Cat eye syndrome and dystonia.
Topics: Adult; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 22; Coloboma; Dystonia | 1996 |
Identification of a cat eye syndrome using DNA sequence dosage analysis.
Topics: Abnormalities, Multiple; Adult; Anus, Imperforate; Chromosome Aberrations; Chromosome Disorders; Chr | 1996 |
Characterization of a derivative chromosome 17 by fish-technique.
Topics: Abnormalities, Multiple; Cerebellum; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Huma | 1996 |
Gillespie syndrome phenotype with a t(X;11)(p22.32;p12) de novo translocation.
Topics: Abnormalities, Multiple; Cerebellum; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Huma | 1998 |
Retinoblastoma in an eye with congenital uveal coloboma.
Topics: Blotting, Southern; Choroid; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair | 1998 |
Aniridia, cataracts, and Wilms tumor.
Topics: Cataract; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Female; Huma | 1978 |
Chromosome analysis techniques expand; new links to cancer.
Topics: Child; Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosomes, Human, 13-15; | 1979 |
Cytogenetic investigation of cat-eye syndrome.
Topics: Adult; Anus, Imperforate; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chr | 1977 |
Ocular findings in triploidy.
Topics: Abnormalities, Multiple; Adolescent; Cataract; Chromosome Aberrations; Chromosome Disorders; Colobom | 1977 |
[Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes].
Topics: Abnormalities, Multiple; Anus, Imperforate; Child, Preschool; Chromosome Aberrations; Chromosome Dis | 1992 |
Fibroblast radiosensitivity and intraocular fibrovascular proliferation following radiotherapy for bilateral retinoblastoma.
Topics: Cell Survival; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Eye Neoplasms; Female; | 1986 |
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 |
Cat eye syndrome associated with aganglionosis of the small and large intestine.
Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 22; Coloboma; Ganglia, Parasy | 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 |
High resolution G-banding analysis in aniridia.
Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Female; Humans; | 1987 |
[Terminal renal failure in aniridia-Wilms syndrome].
Topics: Adult; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 1 | 1986 |
Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entity.
Topics: Abnormalities, Multiple; Adolescent; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Huma | 1987 |
Corneal involvement in autosomal dominant coloboma/microphthalmos.
Topics: Adult; Amblyopia; Chromosome Aberrations; Chromosome Disorders; Coloboma; Cornea; Female; Genes, Dom | 1986 |
The cat eye syndrome.
Topics: Anus, Imperforate; Body Weight; Cephalometry; Chromosome Aberrations; Chromosome Disorders; Chromoso | 1974 |
Autosomal-dominant inheritance of megalocornea associated with down's syndrome.
Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and Y; Congenital Abnormalit | 1974 |
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 |
Some ideas on the time sequence of chromosome function in human organogenesis.
Topics: Choroid; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, 13-15 | 1974 |
Complications in corneal grafting.
Topics: Animals; Antigens; Chromosome Aberrations; Chromosome Disorders; Cornea; Corneal Dystrophies, Heredi | 1972 |
Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree.
Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorder | 1972 |
Short stature, mental retardation and ocular alterations in three siblings.
Topics: Adolescent; Cataract; Child; Chromosome Aberrations; Chromosome Disorders; Eye Diseases; Facial Expr | 1972 |
Congenital cardiac disease and the "cat eye" syndrome.
Topics: Abnormalities, Multiple; Adolescent; Anal Canal; Azygos Vein; Child; Child, Preschool; Choroid; Chro | 1973 |
[Identification of the small submetacentric supernumerary chromosome in the cat's-eye syndrome].
Topics: Adult; Choroid; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Colobo | 1973 |
Reiger's syndrome with chromosomal anomaly (report of a case).
Topics: Abnormalities, Multiple; Adult; Anodontia; Chromosome Aberrations; Chromosome Disorders; Chromosomes | 1973 |
[Cat-eye syndrome].
Topics: Abnormalities, Multiple; Adult; Anal Canal; Child, Preschool; Chromosome Aberrations; Chromosome Dis | 1973 |
[Autosomal dominant irideremia].
Topics: Child; Chromosome Aberrations; Chromosome Disorders; Eye Diseases; Female; Genes, Dominant; Humans; | 1974 |
A new form of albinism.
Topics: Adolescent; Adult; Albinism; Child; Chromosome Aberrations; Chromosome Disorders; Color Perception; | 1974 |
Case report. The cat-eye syndrome with unusual skeletal malformations.
Topics: Abnormalities, Multiple; Anus, Imperforate; Arm; Chromosome Aberrations; Chromosome Disorders; Chrom | 1974 |
[Eye abnormalities of a child with an extra chromosome fragment].
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Coloboma; E | 1968 |
[Frequent familial occurrence of a multiplex malformation of the eye].
Topics: Abnormalities, Multiple; Adult; Blepharoptosis; Child; Child, Preschool; Chromosome Aberrations; Chr | 1971 |
A newborn with the cat-eye syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Anal Canal; Autoradiography; Cells, Cultured; Child; Chi | 1972 |
Dermatoglyphics and chromosomes in cat-eye syndrome.
Topics: Anal Canal; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Coloboma; Dermatoglyphic | 1971 |
Dermatoglyphics and chromosomes in cat-eye syndrome.
Topics: Anal Canal; Chromosome Aberrations; Chromosome Disorders; Coloboma; Dermatoglyphics; Humans; Infant, | 1971 |
Genetical aspects of severe visual impairment in childhood.
Topics: Anophthalmos; Cataract; Child; Child, Preschool; Chorioretinitis; Chromosome Aberrations; Chromosome | 1970 |
[Genetic consultations in ophthalmology].
Topics: Cataract; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Coloboma; Diagnosis | 1969 |
Lester's line in hereditary osteo-onychoysplasia.
Topics: Arm; Chromosome Aberrations; Chromosome Disorders; Female; Humans; Infant; Iris; Leg; Nail-Patella S | 1969 |
[Histopathological study of 2 cases of Leber's congenital tapeto-retinal degeneration].
Topics: Adult; Autopsy; Blindness; Choroid; Chromosome Aberrations; Chromosome Disorders; Ciliary Body; Corn | 1969 |
Human chromosomal deletion: two patients with the 4p- syndrome.
Topics: Abnormalities, Multiple; Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes, | 1970 |
Bilateral colobomas of iris and choroid. Association with partial deletion of a chromosome of group D.
Topics: Abnormalities, Multiple; Choroid; Chromosome Aberrations; Chromosome Disorders; Coloboma; Eye; Human | 1970 |
[The stigmatism of ocular albinism and congenital blindness of Leber. Clinical report].
Topics: Albinism; Blindness; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Genes; Genes, R | 1970 |