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Influence of validating the parental origin on the clinical interpretation of fetal copy number variations in 141 core family cases
BACKGROUND: The sources and variants types of the copy number variations (CNVs) in prenatal fetal, and the critical role of parental origin on the interpretation of fetal CNVs are unclear. METHODS: One hundred and forty‐one prenatal core families with abnormal CNVs were selected and performed by low...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mol Genet Genomic Med |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6785431/ https://ncbi.nlm.nih.gov/pubmed/31475483 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.944 |
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