Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia

Objective: We present prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome (sSMC) derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia. Case report: A 27-year-old woman underwent amniocentesis at 18 weeks of gest...

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Autores principales: Chih-Ping Chen (Autor), Chen-Ju Lin (Autor), Shin-Wen Chen (Autor), Fang-Tzu Wu (Autor), Schu-Rern Chern (Autor), Peih-Shan Wu (Autor), Yun-Yi Chen (Autor), Wen-Lin Chen (Autor), Wayseen Wang (Autor)
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Publicado: Elsevier, 2020-11-01T00:00:00Z.
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