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Reciprocal Translocations in Man. 3:1 Meiotic Disjunction Resulting in 47- or 45-chromosome Offspring

Overview
Journal J Med Genet
Specialty Genetics
Date 1975 Mar 1
PMID 123589
Citations 45
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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.

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References
1.
Ying K . Sporadic (GqGq) translocations in Down's syndrome. Can J Genet Cytol. 1973; 15(2):309-11. DOI: 10.1139/g73-033. View

2.
Hirschhorn K, Lucas M, Wallace I . Precise identification of various chromosomal abnormalities. Ann Hum Genet. 1973; 36(4):375-9. DOI: 10.1111/j.1469-1809.1973.tb00601.x. View

3.
Niebuhr E . Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21. Humangenetik. 1974; 21(1):99-101. DOI: 10.1007/BF00278575. View

4.
Giraud F, Hartung M, Mattei J, Mattie M . [t(7q-; 21q-plus) and familial and trisomy 21]. Ann Genet. 1974; 17(1):49-53. View

5.
Jacobs P, Melville M, Ratcliffe S, KEAY A, Syme J . A cytogenetic survey of 11,680 newborn infants. Ann Hum Genet. 1974; 37(4):359-76. DOI: 10.1111/j.1469-1809.1974.tb01843.x. View