Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient

We report on a phenotypically normal 41-year-old azoospermic man with a 45 chromosomes karyotype including one normal chromosome 21, one normal chromosome 22, and a der(22)ins(22;21). Array CGH showed a 1.8 Mb terminal deletion of bands 21pter to 21q21.1 and a 341 kb terminal deletion on band 21q22....

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發表在:Clin Case Rep
Main Authors: Marquet, Valentine, Bourgeois, Dominique, De Mas, Philippe, Bouneau, Laurence, Vigouroux-Castera, Adeline, Molignier, Romain, Calvas, Patrick
格式: Artigo
語言:Inglês
出版: John Wiley & Sons, Ltd 2015
主題:
Case Reports
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4574793/
https://ncbi.nlm.nih.gov/pubmed/26401282
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.313
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