Inheritance of imbalances in recurrent chromosomal translocation t(11;22): clarification by PGT-SR and sperm-FISH analysis
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynaecology
Reference60 articles.
1. The translocation 11q;22q: a novel unbalanced karyotype;Abeliovich;Am. J. Med. Genet.,1990
2. The Istanbul consensus workshop on embryo assessment: proceedings of an expert meeting;Hum. Reprod.,2011
3. Preferential alternate segregation in the common t(11;22)(q23;q11) reciprocal translocation: sperm FISH analysis in two brothers;Anton;Reprod. Biomed. Online,2004
4. 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;Armstrong;Am. J. Hum. Genet.,2000
5. Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22);Ashley;Am. J. Hum. Genet.,2006
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