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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809756/ https://www.ncbi.nlm.nih.gov/pubmed/33451353 http://dx.doi.org/10.1186/s13039-020-00527-w |