A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
Daw, Sara C.M, Taylor, Catherine, Kraman, Matthew, Call, Kathy, Mao, Jen-i, Schuffenhauer, Simone, Meitinger, Thomas, Lipson, Tony, Goodship, Judith, Scambler, Peter
Published in Nature genetics (01.08.1996)
Published in Nature genetics (01.08.1996)
Get full text
Journal Article
Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome
Halford, S, Wilson, D I, Daw, S C, Roberts, C, Wadey, R, Kamath, S, Wickremasinghe, A, Burn, J, Goodship, J, Mattei, M G
Published in Human molecular genetics (01.10.1993)
Published in Human molecular genetics (01.10.1993)
Get more information
Journal Article
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease
Halford, S, Wadey, R, Roberts, C, Daw, S C, Whiting, J A, O'Donnell, H, Dunham, I, Bentley, D, Lindsay, E, Baldini, A
Published in Human molecular genetics (01.12.1993)
Published in Human molecular genetics (01.12.1993)
Get more information
Journal Article
Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfecta
Williams, E M, Nicholls, A C, Daw, S C, Mitchell, N, Levin, L S, Green, B, MacKenzie, J, Evans, D R, Chudleigh, P A, Pope, F M
Published in Clinical genetics (01.03.1989)
Published in Clinical genetics (01.03.1989)
Get more information
Journal Article