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Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.Journal of Medical Genetics|April 16, 1999
A clinical study of type 1 neurofibromatosis in north west EnglandJ M McGaughran, D I Harris, D Donnai, et al.Journal of Medical Genetics|July 1, 1989
Testing for cystic fibrosis using allelic associationA J Ivinson, A P Read, R Harris, et al.Journal of Medical Genetics|January 1, 1988
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosomeK E Davies, T J Smith, S Bundey, et al.Human Genetics|October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophyA P Read, R C Mountford, S M Forrest, et al.Transplantation|November 1, 1981
Matching for properdin factor B (Bf) in renal transplantationP A Dyer, P T Klouda, R W Johnson, et al.European Journal of Human Genetics : EJHG|May 1, 1997
Linkage analysis in 16 families with incontinentia pigmentiM Jouet, H Stewart, S Landy, et al.Human Molecular Genetics|November 1, 1995
The mutational spectrum in Waardenburg syndromeM Tassabehji, V E Newton, X Z Liu, et al.Journal of Medical Genetics|July 1, 1997
Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3S G Kant, A Van Haeringen, E Bakker, et al.Pageof 19