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Human Genetics
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August 1, 1990
Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus
V J Buckle, J L Guenet, D Simon-Chazottes, et al.
The Indian Journal of Medical Research
|
March 30, 2002
Clinical & genetic analysis of four patients with distal upper limb spinal muscular atrophy
M R Hegde, B Chong, C Stevenson, et al.
Genomics
|
September 1, 1990
Physical mapping distal to the DMD locus
D R Love, J F Bloomfield, S J Kenwrick, et al.
Neuroscience
|
June 1, 1996
Decreased neuronal nitric oxide synthase messenger RNA and somatostatin messenger RNA in the striatum of Huntington's disease
P J Norris, H J Waldvogel, R L Faull, et al.
Internal Medicine Journal
|
April 5, 2013
Novel mutation in the TMEM127 gene associated with phaeochromocytoma
M S Elston, G Y Meyer-Rochow, D Prosser, et al.
Nucleic Acids Research
|
January 11, 1989
Nucleotide sequence of a gene from Caldocellum saccharolyticum encoding for exocellulase and endocellulase activity
D J Saul, L C Williams, D R Love, et al.
Neuroscience
|
August 29, 1998
Trinucleotide (CAG) repeat length is positively correlated with the degree of DNA fragmentation in Huntington's disease striatum
N J Butterworth, L Williams, J Y Bullock, et al.
Genetics and Molecular Research : GMR
|
September 17, 2010
Molecular characterisation of a der(Y)t(Xp;Yp) with Xp functional disomy and sex reversal
F Ashton, R O'Connor, J M Love, et al.
Anesthesia and Analgesia
|
November 1, 1996
A comparison of variable-dose patient-controlled analgesia with fixed-dose patient-controlled analgesia
D R Love, H Owen, A H Ilsley, et al.
Journal of Medical Genetics
|
December 1, 1991
Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy
D R Love, T J Flint, S A Genet, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 9
Human Genetics
|
August 1, 1990
Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus
V J Buckle, J L Guenet, D Simon-Chazottes, et al.
The Indian Journal of Medical Research
|
March 30, 2002
Clinical & genetic analysis of four patients with distal upper limb spinal muscular atrophy
M R Hegde, B Chong, C Stevenson, et al.
Genomics
|
September 1, 1990
Physical mapping distal to the DMD locus
D R Love, J F Bloomfield, S J Kenwrick, et al.
Neuroscience
|
June 1, 1996
Decreased neuronal nitric oxide synthase messenger RNA and somatostatin messenger RNA in the striatum of Huntington's disease
P J Norris, H J Waldvogel, R L Faull, et al.
Internal Medicine Journal
|
April 5, 2013
Novel mutation in the TMEM127 gene associated with phaeochromocytoma
M S Elston, G Y Meyer-Rochow, D Prosser, et al.
Nucleic Acids Research
|
January 11, 1989
Nucleotide sequence of a gene from Caldocellum saccharolyticum encoding for exocellulase and endocellulase activity
D J Saul, L C Williams, D R Love, et al.
Neuroscience
|
August 29, 1998
Trinucleotide (CAG) repeat length is positively correlated with the degree of DNA fragmentation in Huntington's disease striatum
N J Butterworth, L Williams, J Y Bullock, et al.
Genetics and Molecular Research : GMR
|
September 17, 2010
Molecular characterisation of a der(Y)t(Xp;Yp) with Xp functional disomy and sex reversal
F Ashton, R O'Connor, J M Love, et al.
Anesthesia and Analgesia
|
November 1, 1996
A comparison of variable-dose patient-controlled analgesia with fixed-dose patient-controlled analgesia
D R Love, H Owen, A H Ilsley, et al.
Journal of Medical Genetics
|
December 1, 1991
Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy
D R Love, T J Flint, S A Genet, et al.
Page
of 9