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Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome
22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion syndrome in humans. Survival to reproductive age and beyond is now the norm. Several manifestations of this syndrome, such as congenital cardiac disease and neuropsychiatric disorders, may increase risk for adverse pregnancy outc...
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| Veröffentlicht in: | J Genet Couns |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4567324/ https://ncbi.nlm.nih.gov/pubmed/25579115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10897-014-9811-7 |
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