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Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population

BACKGROUND: Genetic causes of male infertility are hypothesized to involve multiple types of mutations, from single gene defects to complex chromosome rearrangements. Recently, several recurrent X-chromosome microdeletions (located in subtelomeric region of the long arm) were reported to be associat...

詳細記述

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書誌詳細
出版年:PLoS One
主要な著者: Chylíková, Blanka, Hrdlička, Ivan, Veselá, Kamila, Řežábek, Karel, Liška, František
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2016
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4892532/
https://ncbi.nlm.nih.gov/pubmed/27257673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0156102
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