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Clinical Science
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October 1, 1971
Plasma renin in idiopathic orthostatic hypotension: differential response in subjects with probable afferent and efferent autonomic failure
D R Love, J J Brown, R H Chinn, et al.
The New Zealand Medical Journal
|
August 23, 1996
DNA-based diagnostics for adrenoleukodystrophy in a large New Zealand family
S A Rowland, A Dodd, A L Roche, et al.
Genomics
|
March 15, 1996
Structure and location of the murine adrenoleukodystrophy gene
M A Kennedy, S A Rowland, A L Miller, et al.
British Journal of Biomedical Science
|
June 29, 2011
Chromosome microarray analysis in a clinical environment: new perspective and new challenge
A George, R Marquis-Nicholson, L T Zhang, et al.
Human Molecular Genetics
|
May 1, 1992
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells
D J Blake, D R Love, J Tinsley, et al.
Nature Genetics
|
June 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1
N G Laing, S D Wilton, P A Akkari, et al.
Nature Genetics
|
January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
N G Laing, S D Wilton, P A Akkari, et al.
Molecular and Cellular Probes
|
October 1, 1995
Molecular characterization of further dystrophin gene microsatellites
S C King, A L Roche, M R Passos-Bueno, et al.
Human Genetics
|
March 1, 1994
A multiple interval physical map of the pericentromeric region of human chromosome 10
A Tunnacliffe, M S Jackson, E Gardner, et al.
British Journal of Cancer
|
September 5, 2001
Analysis of the TGF beta functional pathway in epithelial ovarian carcinoma
K M Francis-Thickpenny, D M Richardson, C C van Ee, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 85) with videos related to
Sort By:
Page
of 9
Clinical Science
|
October 1, 1971
Plasma renin in idiopathic orthostatic hypotension: differential response in subjects with probable afferent and efferent autonomic failure
D R Love, J J Brown, R H Chinn, et al.
The New Zealand Medical Journal
|
August 23, 1996
DNA-based diagnostics for adrenoleukodystrophy in a large New Zealand family
S A Rowland, A Dodd, A L Roche, et al.
Genomics
|
March 15, 1996
Structure and location of the murine adrenoleukodystrophy gene
M A Kennedy, S A Rowland, A L Miller, et al.
British Journal of Biomedical Science
|
June 29, 2011
Chromosome microarray analysis in a clinical environment: new perspective and new challenge
A George, R Marquis-Nicholson, L T Zhang, et al.
Human Molecular Genetics
|
May 1, 1992
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells
D J Blake, D R Love, J Tinsley, et al.
Nature Genetics
|
June 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1
N G Laing, S D Wilton, P A Akkari, et al.
Nature Genetics
|
January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
N G Laing, S D Wilton, P A Akkari, et al.
Molecular and Cellular Probes
|
October 1, 1995
Molecular characterization of further dystrophin gene microsatellites
S C King, A L Roche, M R Passos-Bueno, et al.
Human Genetics
|
March 1, 1994
A multiple interval physical map of the pericentromeric region of human chromosome 10
A Tunnacliffe, M S Jackson, E Gardner, et al.
British Journal of Cancer
|
September 5, 2001
Analysis of the TGF beta functional pathway in epithelial ovarian carcinoma
K M Francis-Thickpenny, D M Richardson, C C van Ee, et al.
Page
of 9