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Biotechnology & Genetic Engineering Reviews
|
January 1, 1985
The molecular genetics of human monogenic diseases
S P Ball, S J Kenwrick, K E Davies
Nucleic Acids Research
|
February 25, 1988
Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping
S J Kenwrick, T J Smith, S England, et al.
Genomics
|
September 1, 1990
Physical mapping distal to the DMD locus
D R Love, J F Bloomfield, S J Kenwrick, et al.
Human Genetics
|
October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophy
A P Read, R C Mountford, S M Forrest, et al.
Nucleic Acids Research
|
March 11, 1987
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients
T J Smith, L Wilson, S J Kenwrick, et al.
Journal of the Royal College of Physicians of London
|
April 1, 1988
Molecular analysis and diagnosis of Duchenne muscular dystrophy
S M Forrest, T J Smith, G S Cross, et al.
American Journal of Medical Genetics
|
March 1, 1988
Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome
K E Davies, M N Patterson, S J Kenwrick, et al.
Journal of Muscle Research and Cell Motility
|
February 1, 1988
Molecular analysis of muscular dystrophy
K E Davies, S J Kenwrick, M N Patterson, et al.
Annals of Clinical Research
|
January 1, 1986
Molecular analysis of X-linked diseases
K E Davies, S P Ball, H R Dorkins, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1986
Molecular analysis of human X-linked diseases
K E Davies, S P Ball, H R Dorkins, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Biotechnology & Genetic Engineering Reviews
|
January 1, 1985
The molecular genetics of human monogenic diseases
S P Ball, S J Kenwrick, K E Davies
Nucleic Acids Research
|
February 25, 1988
Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping
S J Kenwrick, T J Smith, S England, et al.
Genomics
|
September 1, 1990
Physical mapping distal to the DMD locus
D R Love, J F Bloomfield, S J Kenwrick, et al.
Human Genetics
|
October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophy
A P Read, R C Mountford, S M Forrest, et al.
Nucleic Acids Research
|
March 11, 1987
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients
T J Smith, L Wilson, S J Kenwrick, et al.
Journal of the Royal College of Physicians of London
|
April 1, 1988
Molecular analysis and diagnosis of Duchenne muscular dystrophy
S M Forrest, T J Smith, G S Cross, et al.
American Journal of Medical Genetics
|
March 1, 1988
Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome
K E Davies, M N Patterson, S J Kenwrick, et al.
Journal of Muscle Research and Cell Motility
|
February 1, 1988
Molecular analysis of muscular dystrophy
K E Davies, S J Kenwrick, M N Patterson, et al.
Annals of Clinical Research
|
January 1, 1986
Molecular analysis of X-linked diseases
K E Davies, S P Ball, H R Dorkins, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1986
Molecular analysis of human X-linked diseases
K E Davies, S P Ball, H R Dorkins, et al.
Page
of 2