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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2019
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| Materias: | |
| 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 |