Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
Leung, Gordon K C, Mak, Christopher C Y, Fung, Jasmine L F, Wong, Wilfred H S, Tsang, Mandy H Y, Yu, Mullin H C, Pei, Steven L C, Yeung, K S, Mok, Gary T K, Lee, C P, Hui, Amelia P W, Tang, Mary H Y,Volume:
11
Language:
english
Journal:
BMC Medical Genomics
DOI:
10.1186/s12920-018-0409-z
Date:
December, 2018
File:
PDF, 1.21 MB
english, 2018