Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage

Recurrent miscarriage (RM) is a multifactorial disorder with acknowledged genetic heritability that affects ∼3% of couples aiming at childbirth. As copy number variants (CNVs) have been shown to contribute to reproductive disease susceptibility, we aimed to describe genome-wide profile of CNVs and i...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Hum Mutat
Auteurs principaux: Nagirnaja, Liina, Palta, Priit, Kasak, Laura, Rull, Kristiina, Christiansen, Ole B, Nielsen, Henriette S, Steffensen, Rudi, Esko, Tõnu, Remm, Maido, Laan, Maris
Format: Artigo
Langue:Inglês
Publié: BlackWell Publishing Ltd 2014
Sujets:
Research Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4285182/
https://ncbi.nlm.nih.gov/pubmed/24827138
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22589
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires