Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring
- PMID: 123589
- PMCID: PMC1013228
- DOI: 10.1136/jmg.12.1.29
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring
Abstract
Five cases of chromosome imbalance resulting from 3:1 disjunction of reciprocal translocations are described. A review of the literature suggests this phenomenon is more common than has previously been recognized.
Similar articles
-
An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.Hum Hered. 1973;23(6):568-85. doi: 10.1159/000152624. Hum Hered. 1973. PMID: 4134631 No abstract available.
-
Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.Am J Hum Genet. 1975 Jul;27(4):478-85. Am J Hum Genet. 1975. PMID: 125542 Free PMC article.
-
New chromosomal syndromes.Am J Dis Child. 1975 Apr;129(4):515-29. doi: 10.1001/archpedi.1975.02120410075021. Am J Dis Child. 1975. PMID: 124130 No abstract available.
-
Genetics of the +p9 syndrome.Hum Genet. 1976 Apr 15;32(1):23-33. doi: 10.1007/BF00569973. Hum Genet. 1976. PMID: 770307 Review.
-
Human chromosome abnormalities as related to physical and mental dysfunction.J Hered. 1969 Sep-Oct;60(5):239-48. doi: 10.1093/oxfordjournals.jhered.a107981. J Hered. 1969. PMID: 4244249 Review. No abstract available.
Cited by
-
Risk for short arm 10 trisomy. A segregation analysis of eleven families with different translocations.Hum Genet. 1977 Nov 2;39(1):7-13. doi: 10.1007/BF00273148. Hum Genet. 1977. PMID: 924445
-
Partial monosomy 13 and 21 due to a familial 13/21 translocation.Hum Genet. 1978 Apr 24;41(3):243-50. doi: 10.1007/BF00284757. Hum Genet. 1978. PMID: 649151
-
Proximal 15q monosomy.J Med Genet. 1982 Oct;19(5):393-4. doi: 10.1136/jmg.19.5.393-a. J Med Genet. 1982. PMID: 7143400 Free PMC article. No abstract available.
-
Trisomy 9p due to unusual maternal translocation (3;9).J Med Genet. 1984 Aug;21(4):320. doi: 10.1136/jmg.21.4.320. J Med Genet. 1984. PMID: 6492100 Free PMC article. No abstract available.
-
Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.J Med Genet. 1979 Dec;16(6):467-78. doi: 10.1136/jmg.16.6.467. J Med Genet. 1979. PMID: 395305 Free PMC article. Review.
References
MeSH terms
LinkOut - more resources
Full Text Sources