Abnormal meiotic recombination with complex chromosomal rearrangement in an azoospermic man-Reference-Cited by-同舟云学术

Abnormal meiotic recombination with complex chromosomal rearrangement in an azoospermic man

Published:2015-06 Issue:6 Volume:30 Page:651-658
ISSN:1472-6483
Container-title:Reproductive BioMedicine Online
language:en
Short-container-title:Reproductive BioMedicine Online

Author:

Wang Liu,Iqbal Furhan^ORCID,Li Guangyuan,Jiang Xiaohua,Bukhari Ihtisham,Jiang Hanwei,Yang Qingling,Zhong Liangwen,Zhang Yuanwei,Hua Juan,Cooke Howard J.,Shi Qinghua

Funder

National Basic Research Program of China (973)

National Natural Science Foundation of China

Development Foundation of Hefei Center for Physical Science and Technology

Fundamental Research Funds for the Central Universities

Chinese Academy of Sciences

Publisher

Elsevier BV

Subject

Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology

Reference33 articles.

1. Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis;Baarends;Mol. Cell. Biol,2005

2. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype;Bartels;Eur. J. Med. Genet,2007

3. The origin of chromosomal-aberrations in man and their potential for survival and reproduction in the adult human-population;Chandley;Ann. Genet,1981

4. A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I of meiosis;Chandley;Cytogenet. Cell Genet,1986

5. A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: case report;Coco;Hum. Reprod,2004

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