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Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
BACKGROUND: This study aimed to evaluate the applicability of chromosomal microarray analysis (CMA), rather than traditional chromosome analysis, in prenatal diagnosis of ventricular septal defects (VSDs) for superior prenatal genetic counseling and to reveal a potential correlation between submicro...
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| Pubblicato in: | Mol Cytogenet |
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| Autori principali: | , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6264052/ https://ncbi.nlm.nih.gov/pubmed/30519285 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-018-0408-y |
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