Discrimination of Deletion and Duplication Subtypes of the Deleted in Azoospermia Gene Family in the Context of Frequent Interloci Gene Conversion-Reference-Cited by-同舟云学术

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Discrimination of Deletion and Duplication Subtypes of the Deleted in Azoospermia Gene Family in the Context of Frequent Interloci Gene Conversion

Published:2016-10-10 Issue:10 Volume:11 Page:e0163936
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Vaszkó Tibor,Papp János,Krausz Csilla,Casamonti Elena,Géczi Lajos,Olah Edith

Funder

Research Grants NKFI

Norwegian Financial Mechanism’s Norway Grant

Research Grants KTIA-OTKA

Istituto Toscano Tumori grant proposal

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference41 articles.

1. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes;H Skaletsky;Nature,2003

2. The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men;T Kuroda-Kawaguchi;Nat Genet,2001

3. High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia;S Fernandes;Mol Hum Reprod,2002

4. A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N;S Fernandes;Am J Hum Genet,2004

5. Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility;N Machev;J Med Genet,2004

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Correlation between serum levels of reproductive hormones and testicular spermatogenic function in men with azoospermia;Andrologia;2022-08-27

2. Deletions in AZFc Region of Y Chromosome in Russian Fertile Men;Russian Journal of Genetics;2022-07

3. Copy number variants within AZF region of Y chromosome and their association with idiopathic male infertility in Serbian population;Andrologia;2021-10-29

4. Y chromosome structural variation in infertile men detected by targeted next-generation sequencing;Journal of Assisted Reproduction and Genetics;2021-01-16

5. A common 1.6 Mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans;2020-12-09

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