Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2).

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作者信息

Chandley A C

出版信息

Hum Genet. 1992 Sep-Oct;90(1-2):191-2. doi: 10.1007/BF00210779.

DOI:10.1007/BF00210779

PMID:1427783

Abstract

摘要

相似文献

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本文引用的文献

Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11).

Clin Genet. 1984 Apr;25(4):357-61. doi: 10.1111/j.1399-0004.1984.tb02004.x.

Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.

Hum Genet. 1989 Oct;83(3):287-8. doi: 10.1007/BF00285174.

Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3:1 segregation at meiosis I.

Hum Genet. 1990 Jun;85(1):143. doi: 10.1007/BF00276346.

The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.

Hum Genet. 1992 Feb;88(4):482-3. doi: 10.1007/BF00215688.

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