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Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality

Objective: We present prenatal diagnosis of familial transmission of 17q12 duplication associated with no apparent phenotypic abnormality. Case Report: A 36-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age. Cytogenetic analysis revealed a karyotype of...

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Main Authors:	Chih-Ping Chen (Author), Chung-Hu Fu (Author), Yi-Hui Lin (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Yen-Ni Chen (Author), Shin-Wen Chen (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2016-12-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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