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Archives of Disease in Childhood
|
June 1, 1994
Screening for Duchenne muscular dystrophy
J Fenton-May, D M Bradley, J R Sibert, et al.
Human Molecular Genetics
|
April 4, 2002
Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells
Majid Fardaei, Mark T Rogers, Helena M Thorpe, et al.
Journal of Medical Genetics
|
March 1, 1993
A study of DNA methylation in myotonic dystrophy
D J Shaw, S Chaudhary, S A Rundle, et al.
Human Genetics
|
January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus
D J Shaw, A L Meredith, M Sarfarazi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 20, 2006
A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?
A J Murray, T A T Hughes, J W Neal, et al.
The Journal of Physiology
|
May 4, 2004
A role for SNAP-25 but not VAMPs in store-mediated Ca2+ entry in human platelets
Pedro C Redondo, Alan G S Harper, Ginés M Salido, et al.
Social Science & Medicine (1982)
|
February 14, 2006
The "Americanisation" of migrants: evidence for the contribution of ethnicity, social deprivation, lifestyle and life-course processes to the mid-20th century Coronary Heart Disease epidemic in the US
C C Kelleher, J W Lynch, L Daly, et al.
Journal of Medical Genetics
|
November 1, 1992
Minimal expression of myotonic dystrophy: a clinical and molecular analysis
W Reardon, H G Harley, J D Brook, et al.
Clinical Genetics
|
March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratory
L P Lazarou, A L Meredith, J M Myring, et al.
Alimentary Pharmacology & Therapeutics
|
January 22, 2003
Complementary studies of the gastrointestinal safety of the cyclo-oxygenase-2-selective inhibitor etoricoxib
R H Hunt, S Harper, P Callegari, et al.
Page
of 123
Search research articles
Search
Showing results (641-650 of 1,225) with videos related to
Sort By:
Page
of 123
Archives of Disease in Childhood
|
June 1, 1994
Screening for Duchenne muscular dystrophy
J Fenton-May, D M Bradley, J R Sibert, et al.
Human Molecular Genetics
|
April 4, 2002
Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells
Majid Fardaei, Mark T Rogers, Helena M Thorpe, et al.
Journal of Medical Genetics
|
March 1, 1993
A study of DNA methylation in myotonic dystrophy
D J Shaw, S Chaudhary, S A Rundle, et al.
Human Genetics
|
January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus
D J Shaw, A L Meredith, M Sarfarazi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 20, 2006
A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?
A J Murray, T A T Hughes, J W Neal, et al.
The Journal of Physiology
|
May 4, 2004
A role for SNAP-25 but not VAMPs in store-mediated Ca2+ entry in human platelets
Pedro C Redondo, Alan G S Harper, Ginés M Salido, et al.
Social Science & Medicine (1982)
|
February 14, 2006
The "Americanisation" of migrants: evidence for the contribution of ethnicity, social deprivation, lifestyle and life-course processes to the mid-20th century Coronary Heart Disease epidemic in the US
C C Kelleher, J W Lynch, L Daly, et al.
Journal of Medical Genetics
|
November 1, 1992
Minimal expression of myotonic dystrophy: a clinical and molecular analysis
W Reardon, H G Harley, J D Brook, et al.
Clinical Genetics
|
March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratory
L P Lazarou, A L Meredith, J M Myring, et al.
Alimentary Pharmacology & Therapeutics
|
January 22, 2003
Complementary studies of the gastrointestinal safety of the cyclo-oxygenase-2-selective inhibitor etoricoxib
R H Hunt, S Harper, P Callegari, et al.
Page
of 123