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Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing
BACKGROUND: The present study aimed to explore the etiological relationship between fetal abnormalities and copy number variations (CNVs) with the aim of intervening and preventing the birth of children with birth defects in time. METHODS: Samples of 913 fetuses with puncture indications were collec...
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| Publicado no: | J Gene Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8243933/ https://ncbi.nlm.nih.gov/pubmed/33615614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jgm.3324 |
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