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Journal of Medical Genetics|November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophyS Hodgson, K Hart, S Abbs, et al.Journal of Medical Genetics|December 1, 1986
Linkage studies in Duchenne and Becker muscular dystrophiesA Walker, K Hart, C Cole, et al.Clinical Genetics|October 1, 1988
PRUFILE: a clinical and laboratory database for the genetics centreD E Mutton, K Chown, L Thomson, et al.American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.Prenatal Diagnosis|July 1, 1988
Chromosome banding in direct preparations of chorionic villiM Murer-Orlando, J Llerena, M McGuire, et al.Tissue Antigens|May 1, 1975
The search for a human equivalent of the mouse T-locus - negative results from a study of HL-A types in spina bifidaM Bobrow, J G Bodmer, W F Bodmer, et al.Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.Annals of Human Genetics|January 1, 1975
Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13V van Heyningen, M Bobrow, W F Bodmer, et al.Human Genetics|December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.Human Genetics|March 1, 1987
DNA deletions in mild and severe Becker muscular dystrophyK A Hart, S Hodgson, A Walker, et al.Pageof 861