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Two cases of complex balanced autosomal translocations associated with severe oligozoospermia

  • Published:2018-07 Issue: Volume:663 Page:126-130
  • ISSN:0378-1119
  • Container-title:Gene
  • language:en
  • Short-container-title:Gene

Author:

Sha Yan-WeiORCID,Mei Li-Bin,Ji Zhi-Yong,Ding Lu,Ge Yunsheng,Wu Qiong,Kong Hui,Su Zhi-Ying,Li Ping

Funder

Youth Scientific Research Project of Fujian Provincial Health and Family Planning Commission

Science and Technology Project of Fujian Province

Xiamen Science and Technology Planning Project

Major/Important Disease Research Project

Young/Middle-aged Talent Cultivation Project

National Health and Family Planning Commission of the People's Republic of China

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference39 articles.

1. Chromosomal alterations and male infertility;Antonelli;J. Endocrinol. Investig.,2000

2. A rare de novo complex chromosomal rearrangement (CCR) involving four chromosomes in an oligo-asthenosperm infertile man;Asia;Cell J.,2014

3. An excess of chromosome 1 breakpoints in male infertility;Bache;Eur. J. Hum. Genet.,2004

4. Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort;Baptista;Am. J. Hum. Genet.,2008

5. 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

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