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Journal of Medical Genetics|October 1, 1993
Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134)R Wadey, S Daw, A Wickremasinghe, et al.Human Molecular Genetics|June 1, 1995
Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndromeR Wadey, S Daw, C Taylor, et al.Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.American Journal of Human Genetics|November 1, 1992
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndromeA H Carey, D Kelly, S Halford, et al.American Journal of Human Genetics|December 1, 1993
A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21L Wilson, A Curtis, J R Korenberg, et al.American Journal of Medical Genetics|February 1, 1993
Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11D Kelly, R Goldberg, D Wilson, et al.Kidney International|July 1, 2006
Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMDT H J GoodshipHuman Molecular Genetics|October 1, 1993
Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndromeS Halford, D I Wilson, S C Daw, et al.Journal of Inherited Metabolic Disease|January 1, 1994
Relevance of the Human Genome Project to inherited metabolic diseaseJ BurnPageof 58