New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing-Reference-Cited by-同舟云学术

New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing

Published:2017-05-13 Issue:7 Volume:32 Page:1512-1520
ISSN:0268-1161
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Patiño Liliana Catherine,Beau Isabelle,Carlosama Carolina,Buitrago July Constanza,González Ronald,Suárez Carlos Fernando,Patarroyo Manuel Alfonso^ORCID,Delemer Brigitte,Young Jacques,Binart Nadine,Laissue Paul

Funder

Universidad del Rosario

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/32/7/1512/19913988/dex089.pdf

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5. Identification of multiple gene mutations accounts for a new genetic architecture of primary ovarian insufficiency;J Clin Endocrinol Metab,2016

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