Genetics of Congenital Heart Disease: Past and Present-Reference-Cited by-同舟云学术

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Genetics of Congenital Heart Disease: Past and Present

Published:2016-11-02 Issue:2 Volume:55 Page:105-123
ISSN:0006-2928
Container-title:Biochemical Genetics
language:en
Short-container-title:Biochem Genet

Author:

Muntean Iolanda,Togănel Rodica,Benedek Theodora

Funder

University of Medicine and Pharmacy, Tg.Mures, Romania

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s10528-016-9780-7.pdf

Reference121 articles.

1. Ackerman C, Locke AE, Feingold E, Reshey B, Espana K, Thusberg J, Mooney S, Bean LJH, Dooley KJ, Cua CL, Reeves RH, Sherman SL, Maslen CL (2012) An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. Am J Hum Genet 91:646–659

2. Alagille D, Odievre M, Gautier M, Dommergues JP (1975) Hepatic ductular hypoplasia associated with characteristic faces, vertebral malformations, retarded physical, mental and sexual development, and cardiac murmur. J Pediat 86:63–71

3. Andelfinger G (2014) Next-generation sequencing in congenital heart disease: do new brooms sweep clean? J Am Coll Cardiol 64:2507–2509

4. Aoki Y, Niihori T, Kawame H, Kurosawa K, Ohashi H, Tanaka Y, Filocamo M, Kato K, Suzuki Y, Kure S, Matsubara Y (2005) Germline mutations in HRAS proto-oncogene cause Costello syndrome. Nat Genet 37:1038–1040

5. Aoki Y, Niihori T, Banjo T, Okamoto N, Mizuno S, Kurosawa K, Ogata T, Takada F, Yano M, Ando T, Hoshika T, Barnett C et al (2013) Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome. Am J Hum Genet 93:173–180

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