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American Journal of Human Genetics|March 1, 1991
Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative studyG G Consalez, N S Thomas, C L Stayton, et al.American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.Human Genetics|August 1, 1986
Studies of a DNA marker (G8) genetically linked to Huntington disease in British familiesS Youngman, M Sarfarazi, O W Quarrell, et al.Lancet (London, England)|December 5, 1987
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Mutational analysis in X-linked spondyloepiphyseal dysplasia tardaP T Christie, A Curley, M A Nesbit, et al.Nature Genetics|August 1, 1993
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseR G Snell, J C MacMillan, J P Cheadle, et al.Genomics|December 1, 1993
Genomic organization and transcriptional units at the myotonic dystrophy locusD J Shaw, M McCurrach, S A Rundle, et al.Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.American Journal of Human Genetics|April 11, 2001
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14M McEntagart, N Norton, H Williams, et al.Pageof 23