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Paper Details

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Circ Res
101
2019
C607Y, CAMTA2, DLX6, FLT4, FLT4 variants, G200R, Jagged1, Milroy disease, NOTCH, NOTCH1, NOTCH1 locus, NOTCH1 variants, Nonsyndromic Tetralogy of Fallot, PCM1, RYR1, TBX1, TOF, TOF gene, Tetralogy of Fallot, ZFPM1, congenital heart disease, congenital lymphoedema syndrome, cyanotic congenital, heart disease, in-frame indels, loss, missense variants, nonsyndromic, nonsyndromic TOF, patients
Author NameAffiliation
Heather J CordellInstitute of Genetic Medicine, Newcastle University
Mathieu Bourgey
Mathieu Bourgey
Guillaume Bourque
Robert Eveleigh
Graeme C M BlackSaint Mary's Hospital
G M Lathrop
Bernard KeavneyUniversity of Manchester
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