Specific alleles of the PRDM9 gene are a risk factor for the production of chromosomally abnormal embryos in humans

被引：0
|
作者：
Sarasa, J. [1 ]
Enciso, M. [2 ]
Xanthopoulou, L. [3 ]
Bowles, M. [4 ]
Delhanty, J. [3 ]
Wells, D. [2 ]
机构：
[1] Reprogenet UK, Inst Reprod Sci, Oxford, England
[2] Univ Oxford, Reprogenet UK, Inst Reprod Sci, Oxford, England
[3] UCL, Ctr Preimplantat Genet Diag, London, England
[4] Univ Oxford, Inst Reprod Sci, Oxford, England
来源：
HUMAN REPRODUCTION | 2013年 / 28卷
关键词：
D O I：
暂无
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
引用
收藏
页码：108 / 108
页数：1
相关论文
共 4 条
  • [1] Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction
    Borel, Christelle
    Cheung, Fanny
    Stewart, Helen
    Koolen, David A.
    Phillips, Christopher
    Thomas, N. Simon
    Jacobs, Patricia A.
    Eliez, Stephan
    Sharp, Andrew J.
    HUMAN GENETICS, 2012, 131 (09) : 1519 - 1524
  • [2] Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest
    Toshinobu Miyamoto
    Eitetsu Koh
    Naoko Sakugawa
    Hisashi Sato
    Hiroaki Hayashi
    Mikio Namiki
    Kazuo Sengoku
    Journal of Assisted Reproduction and Genetics, 2008, 25 : 553 - 557
  • [3] Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest
    Miyamoto, Toshinobu
    Koh, Eitetsu
    Sakugawa, Naoko
    Sato, Hisashi
    Hayashi, Hiroaki
    Namiki, Mikio
    Sengoku, Kazuo
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2008, 25 (11-12) : 553 - 557
  • [4] Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction
    Christelle Borel
    Fanny Cheung
    Helen Stewart
    David A. Koolen
    Christopher Phillips
    N. Simon Thomas
    Patricia A. Jacobs
    Stephan Eliez
    Andrew J. Sharp
    Human Genetics, 2012, 131 : 1519 - 1524
1