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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Vydáno v:Mol Cytogenet
Hlavní autoři: Zhang, Xinyue, Yue, Fagui, Shi, Qingyang, Jiang, Yuting, He, Jing, Li, Leilei, Liu, Ruizhi
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2021
Témata:
Case Report
On-line přístup: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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