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Genomics|December 1, 1991
A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneityW Reardon, H R Middleton-Price, L Sandkuijl, et al.Cardiovascular Research|September 1, 2001
A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen syndromeL Huang, M Bitner-Glindzicz, L Tranebjaerg, et al.British Journal of Audiology|April 1, 1992
Clinical and genetic heterogeneity in X-linked deafnessW Reardon, H R Middleton-Price, S Malcolm, et al.Journal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.Diabetic Medicine : a Journal of the British Diabetic Association|February 1, 1990
Non-mydriatic retinal photography as a screening service for general practitionersD Rogers, M Bitner-Glindzicz, C Harris, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Inheritance of parental chromosomes 15 in Angelman syndrome--implications for the familyT Webb, S Malcolm, M E Pembrey, et al.Journal of Medical Genetics|January 1, 1988
Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophyJ Goodship, S Malcolm, M E Robertson, et al.Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.Human Genetics|February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndromeJ C Smith, T Webb, M E Pembrey, et al.Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.Pageof 96