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Human Genetics
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August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy
K V Walsh, H G Harley, J D Brook, et al.
The British Journal of Ophthalmology
|
September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosis
W Reardon, J C MacMillan, J Myring, et al.
Lancet (London, England)
|
May 9, 1992
Unstable DNA sequence in myotonic dystrophy
H G Harley, S A Rundle, W Reardon, et al.
Journal of Medical Genetics
|
February 1, 1991
Identification of new DNA markers close to the myotonic dystrophy locus
J D Brook, H G Harley, K V Walsh, et al.
Nature
|
February 6, 1992
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
H G Harley, J D Brook, S A Rundle, et al.
American Journal of Human Genetics
|
July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker
H G Harley, J D Brook, J Floyd, et al.
Genomics
|
June 1, 1992
Radiation-reduced hybrids for the myotonic dystrophy locus
J D Brook, B V Zemelman, K Hadingham, 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 dystrophy
H G Harley, S A Rundle, J C MacMillan, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19
A Mitchell, A E Bale, B J Lee, et al.
Human Genetics
|
May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments
J D Brook, S J Knight, S H Roberts, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Human Genetics
|
August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy
K V Walsh, H G Harley, J D Brook, et al.
The British Journal of Ophthalmology
|
September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosis
W Reardon, J C MacMillan, J Myring, et al.
Lancet (London, England)
|
May 9, 1992
Unstable DNA sequence in myotonic dystrophy
H G Harley, S A Rundle, W Reardon, et al.
Journal of Medical Genetics
|
February 1, 1991
Identification of new DNA markers close to the myotonic dystrophy locus
J D Brook, H G Harley, K V Walsh, et al.
Nature
|
February 6, 1992
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
H G Harley, J D Brook, S A Rundle, et al.
American Journal of Human Genetics
|
July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker
H G Harley, J D Brook, J Floyd, et al.
Genomics
|
June 1, 1992
Radiation-reduced hybrids for the myotonic dystrophy locus
J D Brook, B V Zemelman, K Hadingham, 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 dystrophy
H G Harley, S A Rundle, J C MacMillan, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19
A Mitchell, A E Bale, B J Lee, et al.
Human Genetics
|
May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments
J D Brook, S J Knight, S H Roberts, et al.
Page
of 3