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American Journal of Human Genetics|October 1, 1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneityD A Collier, T G Barrett, D Curtis, et al.Nature Genetics|October 1, 1993
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathyZ Y Chen, E M Battinelli, A Fielder, et al.Human Molecular Genetics|June 1, 1997
A novel mechanism of aberrant pre-mRNA splicing in humansJ D Cogan, M A Prince, S Lekhakula, et al.American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.Journal of the Neurological Sciences|July 1, 1978
A genetic study of subacute and chronic spinal muscular atrophy in childhood. A nosological analysis of 124 index patientsJ Pearn, S Bundley, C O Carter, et al.Journal of Medical Genetics|August 1, 1982
A three generation family study of cleft lip with or without cleft palateC O Carter, K Evans, R Coffey, et al.Journal of Medical Genetics|October 1, 1982
A family study of isolated cleft palateC O Carter, K Evans, R Coffey, et al.Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.Pageof 8