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Prenatal detection and molecular cytogenetic characterization of 19q13.42 microduplication: three reported cases and literature review
BACKGROUND: Trisomy 19q is a recognizable syndrome and associated with a wide spectrum of clinical phenotypes in clinic. The purpose of this study was to explore the prenatal phenotypes of 19q13.42 duplication, which was rarely reported in clinic. CASE PRESENTATION: Three pregnant women presenting d...
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| Publicado no: | Mol Cytogenet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7809756/ https://ncbi.nlm.nih.gov/pubmed/33451353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-020-00527-w |
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