Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)-Reference-Cited by-同舟云学术

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

Published:2018-10-25 Issue:1 Volume:11 Page:
ISSN:1755-8794
Container-title:BMC Medical Genomics
language:en
Short-container-title:BMC Med Genomics

Author:

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,Chan Kelvin Y K,Liu Anthony P Y,Yang Wanling,Sham P C,Kan Anita S Y,Chung Brian H Y^ORCID

Funder

Health and Medical Research Fund

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12920-018-0409-z.pdf

Reference33 articles.

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2. Stengel-Rutkowski S, et al. Routine G-banding in prenatal diagnosis of chromosomal disorders. Hum Genet. 1976;31(2):231–4.

3. Wapner RJ, et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med. 2012;367(23):2175–84.