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-Reference-Cited by-同舟云学术

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

Published:2005 Issue:8 Volume:25 Page:683-686
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Jobanputra Vaidehi,Chung Wendy K.,Hacker April M.,Emanuel Beverly S.,Warburton Dorothy

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference29 articles.

1. The translocation 11q;22q: A novel unbalanced karyotype

2. 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

3. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories

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

5. AT-Rich Palindromes Mediate the Constitutional t(11;22) Translocation

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