David I. Wilson

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

A K Ryan, Judith A. Goodship, David I. Wilson et al. · Journal of Medical Genetics · 1997 · 1.2K citations · Full text

Cytogenetics, Genetics, Genetic Epidemiology +23

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Newbury-Ecob Ra, David I. Wilson, T Strachan et al. · Nature Genetics · 1997 · 925 citations

Developmental Anomaly, Genetic Disorder, Genetics +6

DiGeorge syndrome: part of CATCH 22.

David I. Wilson, John Burn, Peter Scambler et al. · Journal of Medical Genetics · 1993 · 511 citations · Full text

Genetics, Pathology, Congenital Heart Anomaly +17

Endoglin, an Ancillary TGFβ Receptor, Is Required for Extraembryonic Angiogenesis and Plays a Key Role in Heart Development

Helen M. Arthur, Jan Ure, Andrew J. H. Smith et al. · Developmental Biology · 2000 · 435 citations

Angiogenesis, Developmental Biology, Extraembryonic Angiogenesis +12

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

Peter Scambler, David A. Kelly, Elizabeth Lindsay et al. · The Lancet · 1992 · 418 citations

Genetic Disorder, Genetics, Pathology +7