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Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families

We have previously shown an extensive load of somatic copy number variations (CNVs) in the human placental genome with the highest fraction detected in normal term pregnancies. Hereby, we hypothesized that insufficient promotion of CNVs may impair placental development and lead to recurrent pregnanc...

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Detalles Bibliográficos
Autores principales:	Kasak, Laura, Rull, Kristiina, Sõber, Siim, Laan, Maris
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366903/ https://www.ncbi.nlm.nih.gov/pubmed/28345611 http://dx.doi.org/10.1038/srep45327

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