Literature DB >> 2358300

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

R H Lindenbaum.   

Abstract

Mesh：

Year:  1990        PMID： 2358300     DOI： 10.1007/bf00276346

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  4 in total

1.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

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

Authors:  D H Lockwood; A Farrier; F Hecht; J Allanson
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

3.  The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families.

Authors:  L Iselius; J Lindsten; A Aurias; M Fraccaro; C Bastard; A M Bottelli; T H Bui; D Caufin; L Dalprà; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Comparative mapping of the constitutional and tumor-associated 11;22 translocations.

Authors:  M Budarf; B Sellinger; C Griffin; B S Emanuel
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025
  4 in total
  4 in total

1.  Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors:  S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

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

Authors:  A C Chandley
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

3.  A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.

Authors:  Vaidehi Jobanputra; Wendy K Chung; April M Hacker; Beverly S Emanuel; Dorothy Warburton
Journal:  Prenat Diagn       Date:  2005-08       Impact factor: 3.050

4.  Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

Authors:  A J Dawson; A J Mears; A E Chudley; T Bech-Hansen; H McDermid
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318
  4 in total

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