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The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy
BACKGROUND: The implementation of molecular karyotyping has resulted in an improved diagnostic yield in the genetic diagnostics of congenital anomalies, detected prenatally or after the termination of pregnancy. However, the systematic epidemiologic ascertainment of copy number variations in the eti...
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| Vydáno v: | Mol Genet Genomic Med |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6565594/ https://ncbi.nlm.nih.gov/pubmed/31004418 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.658 |
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