Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants-Reference-Cited by-同舟云学术

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Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants

Published:2014-12-11 Issue:4 Volume:21 Page:339-346
ISSN:1460-2407
Container-title:MHR: Basic science of reproductive medicine
language:en
Short-container-title:

Author:

Filges I.,Manokhina I.,Peñaherrera M.S.,McFadden D.E.,Louie K.,Nosova E.,Friedman J.M.,Robinson W.P.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynaecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

Link

http://academic.oup.com/molehr/article-pdf/21/4/339/16839223/gau112.pdf

Reference56 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat Methods,2010

2. The GTPase Gem and its partner Kif9 are required for chromosome alignment, spindle length control, and mitotic progression;Andrieu;FASEB J,2012

3. Expression of CSF-1/c-fms and SF/c-kit mRNA during preimplantation mouse development;Arceci;Dev Biol,1992

4. Defective calcium release during in vitro fertilization of maturing oocytes of LT/Sv mice;Archacka;Int J Dev Biol,2008

5. The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders;Bourque;Clin Genet,2011

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