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...

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Detalles Bibliográficos
Autores principales: Nagirnaja, Liina, Palta, Priit, Kasak, Laura, Rull, Kristiina, Christiansen, Ole B, Nielsen, Henriette S, Steffensen, Rudi, Esko, Tõnu, Remm, Maido, Laan, Maris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285182/
https://www.ncbi.nlm.nih.gov/pubmed/24827138
http://dx.doi.org/10.1002/humu.22589

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285182/
https://www.ncbi.nlm.nih.gov/pubmed/24827138
http://dx.doi.org/10.1002/humu.22589

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