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Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot
Chen, Chih-Ping, Chen, Chen-Yu, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Yen-Ni, Chen, Shin-Wen, Chen, Li-Feng, Yang, Chien-Wen, Wang, WayseenVolume:
55
Language:
english
Journal:
Taiwanese Journal of Obstetrics and Gynecology
DOI:
10.1016/j.tjog.2016.02.013
Date:
April, 2016
File:
PDF, 825 KB
english, 2016