Beau Crabb

The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants

Katrina Tatton‐Brown, Anna Zachariou, Chey Loveday et al. · Wellcome Open Research · 2018 · 106 citations · Full text

Chimerism for 20q11.2 microdeletion of <i>GDF5</i> explains discordant phenotypes in monochorionic‐diamniotic twins

Matthew M. Meredith, Beau Crabb, Marcelo Alves Vargas et al. · American Journal of Medical Genetics Part A · 2017 · 38 citations

Whole Exome Sequencing, Familial Genomic Triangulation, and Systems Biology Converge to Identify a Novel Nonsense Mutation in<i>TAB2-</i>encoded TGF-beta Activated Kinase 1 in a Child with Polyvalvular Syndrome

Jaeger P. Ackerman, John Smestad, David J. Tester et al. · Congenital Heart Disease · 2016 · 18 citations