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Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry

✍ Scribed by Chen, Chih-Ping; Chen, Ming; Chen, Chen-Yu; Chern, Schu-Rern; Wu, Peih-Shan; Chang, Shun-Ping; Kuo, Yu-Ling; Chen, Wen-Lin; Pan, Chen-Wen; Wang, Wayseen

Book ID: 122162729
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 643 KB
Volume: 536
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.12.036

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