Functional consequences of copy number variants in miscarriage

BACKGROUND: The presence of unique copy number variations (CNVs) in miscarriages suggests that their integral genes have a role in maintaining early pregnancy. In our previous work, we identified 19 unique CNVs in ~40% of studied euploid miscarriages, which were predominantly familial in origin. In...

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Detalles Bibliográficos
Autores principales: Wen, Jiadi, Hanna, Courtney W, Martell, Sally, Leung, Peter CK, Lewis, Suzanne ME, Robinson, Wendy P, Stephenson, Mary D, Rajcan-Separovic, Evica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324423/
https://www.ncbi.nlm.nih.gov/pubmed/25674159
http://dx.doi.org/10.1186/s13039-015-0109-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324423/
https://www.ncbi.nlm.nih.gov/pubmed/25674159
http://dx.doi.org/10.1186/s13039-015-0109-8

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