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The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease

author

Sally L. Dunwoodie

Gillian M Blue

Justin Szot

Gavin Chapman

Edwin P. Kirk

Richard P. Harvey

David Winlaw

published in: International Journal of Cardiology

date of publication: 2016-12-13

language: English

main subject: congenital disorder

Cites articles 4

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2013-05-26

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

Diana Zelenika, Mark Lathrop, Chrysovalanto Mamasoula, Darroch Hall, David Winlaw, Michiel E. Adriaens, Alex V Postma, Marc Gewillig, Shoumo Bhattacharya, Bernard Keavney, Judith A Goodship, Javier T Granados-Riveron, Heather Cordell, Jamie Bentham, Catherine Cosgrove, Jeroen Breckpot, Kerry Setchfield, Chris Thornborough, Rachel Soemedi, Ana Töpf, Thahira Rahman, Gillian M Blue, Simon Heath, Aelko H. Zwinderman, Seema Mital, Antoon F. M. Moorman, Martin Farrall, Klaartje van Engelen, Koen Devriendt
2012-11-01

An integrated map of genetic variation from 1,092 human genomes

Gilean McVean, Gonçalo Abecasis, Richard M. Durbin, Adam Auton, Robert E Handsaker, Vineet Bafna, Klaudia Walter, Andrew G. Clark, Andrea Angius, Matthew Hurles, Gabor T Marth
2005-09-08

Mutations in NOTCH1 cause aortic valve disease

Vidu Garg, Paul Grossfeld
1991-11-01

Specific EGF repeats of Notch mediate interactions with Delta and serrate: Implications for notch as a multifunctional receptor

Article - wd:Q39090901

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