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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.
Breast Cancer Research and Treatment
|
February 24, 2001
Loss of heterozygosity in bilateral breast cancer
J Kollias, S Man, M Marafie, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1991
Exon amplification: a strategy to isolate mammalian genes based on RNA splicing
A J Buckler, D D Chang, S L Graw, et al.
Clinical Genetics
|
April 1, 1993
The DM mutation; diagnostic applications in the Finnish population
P Nokelainen, P Shelbourne, D Shaw, et al.
British Medical Journal (Clinical Research Ed.)
|
November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy
A L Meredith, S M Huson, P W Lunt, et al.
Human Genetics
|
November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19
D J Shaw, A L Meredith, J D Brook, et al.
Genomics
|
January 16, 1999
Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19
C H Yi, J A Terrett, Q Y Li, 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.
Human Genetics
|
May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q
H G Harley, K V Walsh, S 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.
Page
of 8
Search research articles
Search
Showing results (51-60 of 72) with videos related to
Sort By:
Page
of 8
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.
Breast Cancer Research and Treatment
|
February 24, 2001
Loss of heterozygosity in bilateral breast cancer
J Kollias, S Man, M Marafie, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1991
Exon amplification: a strategy to isolate mammalian genes based on RNA splicing
A J Buckler, D D Chang, S L Graw, et al.
Clinical Genetics
|
April 1, 1993
The DM mutation; diagnostic applications in the Finnish population
P Nokelainen, P Shelbourne, D Shaw, et al.
British Medical Journal (Clinical Research Ed.)
|
November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy
A L Meredith, S M Huson, P W Lunt, et al.
Human Genetics
|
November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19
D J Shaw, A L Meredith, J D Brook, et al.
Genomics
|
January 16, 1999
Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19
C H Yi, J A Terrett, Q Y Li, 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.
Human Genetics
|
May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q
H G Harley, K V Walsh, S 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.
Page
of 8