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Nucleic Acids Research
|
May 27, 1986
An XmnI RFLP at the subtelomeric Xp locus DXS31 [HGM7, LA, 1985]
K Wrogemann, M Koenig, Y Alembik, et al.
American Journal of Human Genetics
|
August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
C R Greenberg, J L Hamerton, M Nigli, et al.
Fertility and Sterility
|
August 1, 1993
Partial androgen insensitivity--are all tissues equal?
E J Keely, D D Belsham, K Wrogemann, et al.
Biochimica Et Biophysica Acta
|
January 23, 1985
Functional studies on in situ-like mitochondria isolated in the presence of polyvinyl pyrrolidone
K Wrogemann, E G Nylen, I Adamson, et al.
Muscle & Nerve
|
August 1, 1988
Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy
M J Glesby, E Rosenmann, E G Nylen, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1993
Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome
F A Pereira, E Rosenmann, E G Nylen, et al.
American Journal of Medical Genetics
|
April 1, 1991
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction
C R Greenberg, H K Jacobs, W Halliday, et al.
Journal of the Neurological Sciences
|
October 1, 1992
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy
D D Belsham, W C Yee, C R Greenberg, et al.
Pediatric Research
|
September 1, 1978
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease
S D Pena, N M Quilliam, J L Hamerton, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1993
Single-blind study of dystrophin staining in carriers of Duchenne muscular dystrophy
F P Bernier, C R Greenberg, W C Halliday, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Nucleic Acids Research
|
May 27, 1986
An XmnI RFLP at the subtelomeric Xp locus DXS31 [HGM7, LA, 1985]
K Wrogemann, M Koenig, Y Alembik, et al.
American Journal of Human Genetics
|
August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
C R Greenberg, J L Hamerton, M Nigli, et al.
Fertility and Sterility
|
August 1, 1993
Partial androgen insensitivity--are all tissues equal?
E J Keely, D D Belsham, K Wrogemann, et al.
Biochimica Et Biophysica Acta
|
January 23, 1985
Functional studies on in situ-like mitochondria isolated in the presence of polyvinyl pyrrolidone
K Wrogemann, E G Nylen, I Adamson, et al.
Muscle & Nerve
|
August 1, 1988
Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy
M J Glesby, E Rosenmann, E G Nylen, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1993
Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome
F A Pereira, E Rosenmann, E G Nylen, et al.
American Journal of Medical Genetics
|
April 1, 1991
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction
C R Greenberg, H K Jacobs, W Halliday, et al.
Journal of the Neurological Sciences
|
October 1, 1992
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy
D D Belsham, W C Yee, C R Greenberg, et al.
Pediatric Research
|
September 1, 1978
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease
S D Pena, N M Quilliam, J L Hamerton, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1993
Single-blind study of dystrophin staining in carriers of Duchenne muscular dystrophy
F P Bernier, C R Greenberg, W C Halliday, et al.
Page
of 8