2-propanol has been researched along with Chromosomal Translocation in 18 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 association of moderate mental retardation, behavioural problems, macrocephaly, dysmorphic features with iris coloboma, and supernumerary nipples was observed in two brothers with a terminal deletion 4q33-->4qter and a terminal duplication 7q34-->7qter." | 1.32 | Familial cryptic translocation with deletion 4q33-->4qter and duplication 7q34-->7qter in brothers with mental retardation, macrocephaly and iris coloboma. ( Driessen, SD; Engelen, JJ; Fryns, JP; Moog, U; van Schrojenstein Lantman-de Valk, HM, 2003) |
| "A newborn with partial trisomy 2q, due to a maternal (2;6) translocation is presented." | 1.27 | Corneal pathology and aniridia associated with partial trisomy 2q, due to a maternal (2;6) translocation. ( Clarke, WN; Clifford, BG; Cox, DM; Hunter, AG; MacDonald, IM; Reid, JC, 1984) |
| "The child has mild developmental delay, coloboma of the right eye, and Hirschsprung's disease." | 1.27 | Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22). ( Campbell, NT; Keith, CG; Webb, GC, 1988) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 14 (77.78) | 18.7374 |
| 1990's | 3 (16.67) | 18.2507 |
| 2000's | 1 (5.56) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Moog, U | 1 |
| Engelen, JJ | 1 |
| van Schrojenstein Lantman-de Valk, HM | 1 |
| Driessen, SD | 1 |
| Fryns, JP | 2 |
| Petit, P | 1 |
| Godart, S | 1 |
| Simola, KO | 2 |
| Knuutila, S | 1 |
| Kaitila, I | 1 |
| Pirkola, A | 1 |
| Pohja, P | 1 |
| Yunis, JJ | 1 |
| Lewandowski, RC | 1 |
| Jaeger, EA | 1 |
| MacDonald, IM | 1 |
| Clarke, WN | 1 |
| Clifford, BG | 1 |
| Reid, JC | 1 |
| Cox, DM | 1 |
| Hunter, AG | 1 |
| Clark, CE | 1 |
| Telfer, MA | 1 |
| Cowell, HR | 1 |
| Kalamchi, A | 1 |
| Steg, NL | 1 |
| Abeliovich, D | 1 |
| Yagupsky, P | 1 |
| Bashan, N | 1 |
| Gödde-Salz, E | 1 |
| Behnke, H | 1 |
| Ramesh, KH | 1 |
| Shah, HO | 1 |
| Sherman, J | 1 |
| Lin, JH | 1 |
| Verma, RS | 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 |
| Kozma, C | 1 |
| Hunt, M | 1 |
| Meck, J | 1 |
| Traboulsi, E | 1 |
| Scribanu, N | 1 |
| Gessler, M | 1 |
| Bruns, GA | 1 |
| Seawright, A | 1 |
| Fletcher, JM | 1 |
| Fantes, JA | 1 |
| Morrison, H | 1 |
| Porteous, DJ | 1 |
| Li, SS | 1 |
| Hastie, ND | 1 |
| Van Heyningen, V | 1 |
| Davis, LM | 2 |
| Stallard, R | 1 |
| Thomas, GH | 2 |
| Couillin, P | 1 |
| Junien, C | 1 |
| Nowak, NJ | 2 |
| Shows, TB | 2 |
| Byers, MG | 1 |
| Fukushima, Y | 1 |
| Qin, SZ | 1 |
| Scoggin, C | 1 |
| Webb, GC | 1 |
| Keith, CG | 1 |
| Campbell, NT | 1 |
| Moore, JW | 1 |
| Hyman, S | 1 |
| Antonarakis, SE | 1 |
| Mules, EH | 1 |
1 review available for 2-propanol and Chromosomal Translocation
| Article | Year |
|---|---|
High-resolution cytogenetics.
Topics: Adolescent; Chromosome Aberrations; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, 13- | 1983 |
17 other studies available for 2-propanol and Chromosomal Translocation
| Article | Year |
|---|---|
Familial cryptic translocation with deletion 4q33-->4qter and duplication 7q34-->7qter in brothers with mental retardation, macrocephaly and iris coloboma.
Topics: Abnormalities, Multiple; Adult; Chromosomes, Human, Pair 4; Chromosomes, Human, Pair 7; Coloboma; Ge | 2003 |
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 |
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 |
Ocular findings in Down's syndrome.
Topics: Adolescent; Adult; Aged; Cataract; Chromosomes, Human, 21-22 and Y; Down Syndrome; Eye Diseases; Fem | 1980 |
Corneal pathology and aniridia associated with partial trisomy 2q, due to a maternal (2;6) translocation.
Topics: Chromosomes, Human, 1-3; Chromosomes, Human, 6-12 and X; Cornea; Corneal Diseases; Female; Genetic C | 1984 |
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 |
3:1 meiotic disjunction in a mother with a balanced translocation, 46,XX,t(5,14)(p15;q13) resulting in tertiary trisomy and tertiary monosomy offspring.
Topics: Adult; Alleles; Chromosome Deletion; Chromosomes, Human, 13-15; Chromosomes, Human, 4-5; Coloboma; D | 1982 |
Aniridia, mental retardation and an unbalanced reciprocal translocation of chromosomes 8 and 11 with an interstitial deletion of 11p.
Topics: Adult; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, 6-12 and X; Female; Humans; Inte | 1981 |
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 |
Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye.
Topics: Abnormalities, Multiple; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 4; Eye Abnormalities; | 1990 |
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 |
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 |
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 |
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 |
Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).
Topics: Abnormalities, Multiple; Adult; Child, Preschool; Chromosome Banding; Chromosome Deletion; Chromosom | 1988 |
Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Banding; Chromosome Deletion; Chromosomes, Hum | 1986 |