A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21

Human nondisjunction errors in oocytes are the leading cause of pregnancy loss, and for pregnancies that continue to term, the leading cause of intellectual disabilities and birth defects. For the first time, we have conducted a candidate gene and genome-wide association study to identify genes asso...

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Detalles Bibliográficos
Autores principales: Chernus, Jonathan M., Allen, Emily G., Zeng, Zhen, Hoffman, Eva R., Hassold, Terry J., Feingold, Eleanor, Sherman, Stephanie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932832/
https://www.ncbi.nlm.nih.gov/pubmed/31830031
http://dx.doi.org/10.1371/journal.pgen.1008414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932832/
https://www.ncbi.nlm.nih.gov/pubmed/31830031
http://dx.doi.org/10.1371/journal.pgen.1008414

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