S. C. M. Daw

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

S. C. M. Daw, Catherine Taylor, Matthew Kraman et al. · Nature Genetics · 1996 · 219 citations

Medicine, Cardiology, Molecular Medicine +6

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

Stephanle Halford, Roy Wadey, Catherine Roberts et al. · Human Molecular Genetics · 1993 · 140 citations

Life Sciences, Genetics, Molecular Genetics +14

Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci

Sue Ann Berend, Aimee S. Spikes, Catherine D. Kashork et al. · American Journal of Medical Genetics · 2000 · 72 citations

Life Sciences, Genetics, Molecular Genetics +15

Cloning and Developmental Expression Analysis of Chick Hira (Chira), a Candidate Gene for DiGeorge Syndrome

C.J. Roberts, S. C. M. Daw, Stephanie Halford et al. · Human Molecular Genetics · 1997 · 65 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

Roy Wadey, S. C. M. Daw, Catherine Taylor et al. · Human Molecular Genetics · 1995 · 59 citations

Life Sciences, Genetics, Molecular Genetics +8