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Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects

✍ Scribed by Kuo, Yu-Ling; Chen, Chih-Ping; Wang, Liang-Kai; Ko, Tsang-Ming; Chang, Tung-Yao; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Yu-Ting; Chang, Shu-Yuan

Book ID: 125794573
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 520 KB
Volume: 53
Category: Article
ISSN: 1028-4559
DOI: 10.1016/j.tjog.2014.04.021

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