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P S Harper

Showing results (201-210 of 216) with videos related to

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American Journal of Human Genetics|July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA markerH G Harley, J D Brook, J Floyd, et al.
Genomics|November 1, 1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locusH G Harley, J D Brook, C L Jackson, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
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.
Pageof 22

Showing results (201-210 of 216) with videos related to

Sort By:
Pageof 22
American Journal of Human Genetics|July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA markerH G Harley, J D Brook, J Floyd, et al.
Genomics|November 1, 1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locusH G Harley, J D Brook, C L Jackson, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
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.
Pageof 22