Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease |
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| Authors: | Halford, Stephanle Wadey, Roy Roberts, Catherine Daw, Sara C.M. Whiting, Jennifer A. O'Donnell, Hllary Dunham, Ian Bentley, David Lindsay, Elizabeth BaldInI, Antonio Francis, Fiona Lehrach, Hans Williamson, Robert Wilson, David I. Goodship, Judith Cross, Ian Burn, John Scambler, Peter J. |
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| Affiliation: | Molecular Medicine Unit, Institute of Child Health Guilford Street, London WC1N 1EH, UK 1Division of Medical and Molecular Genetics, UMDS Guy's Tower, London SE1 9RT, UK 2T936 Molecular Genetics Institute, Baylor College of Medicine Houston TX 77030, USA 3Genome Analysis Laboratory, ICRF Lincoln's Inn Fields, London WC2A 3PX, UK 4Department of Biochemistry and Molecular Genetics, St Mary's Hospital Medical School, Imperial College London W2 1PG, UK 5Division of Human Genetics, 19, Claremont Place, University of Newcastle upon Tyne Newcastle upon Tyne NE2 4AA, UK +These authors made an equal contribution to this work and are listed alphabetically |
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