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Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies
The association between genetics and fetuses with ventriculomegaly (VM) is unknown. This study aimed to classify and evaluate abnormal copy number variations (CNVs) in fetuses with VM. From December 2016 to September 2020, amniotic fluid or umbilical cord blood from 293 pregnant women carrying fetus...
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| Pubblicato in: | Front Genet |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8286336/ https://ncbi.nlm.nih.gov/pubmed/34285689 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.682707 |
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