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A M Kessling

Showing results (1-10 of 39) with videos related to

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Ciba Foundation Symposium|January 1, 1990
The problem of polygenic diseaseR Williamson, A M Kessling
Human Genetics|September 16, 1998
MTHFR association with arteriosclerotic vascular disease?O Fletcher, A M Kessling
Lancet (London, England)|August 31, 1985
Interpretation of presence of S2 alleleA M Kessling, S E Humphries
Clinical Genetics|October 1, 1985
A study of DNA polymorphisms around the human apolipoprotein AI gene in hyperlipidaemic and normal individualsA M Kessling, B Horsthemke, S E Humphries
Atherosclerosis|January 5, 1996
Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a 'null' LDL-receptor gene defectC Bétard, A M Kessling, M Roy, et al.
British Journal of Urology|November 7, 1998
Genetic initiation, progression and prognostic markers in transitional cell carcinoma of the bladder: a summary of the structural and transcriptional changes, and the role of developmental genesJ M Adshead, A M Kessling, C W Ogden
Ciba Foundation Symposium|January 1, 1987
Use of DNA polymorphisms of the apolipoprotein genes to study the role of genetic variation in the determination of serum lipid levelsS E Humphries, P J Talmud, A M Kessling
Clinical Genetics|June 1, 1986
DNA polymorphisms around the apo AI gene in normal and hyperlipidaemic individuals selected for a twin studyA M Kessling, K Berg, E Mockleby, et al.
Genomics|May 18, 1999
Novel methodology for the detection of chromosome 21-specific alpha-satellite DNA sequencesK Maratou, Y Siddique, A M Kessling, et al.
Human Genetics|July 29, 2000
Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunctionK Maratou, Y Siddique, A M Kessling, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Ciba Foundation Symposium|January 1, 1990
The problem of polygenic diseaseR Williamson, A M Kessling
Human Genetics|September 16, 1998
MTHFR association with arteriosclerotic vascular disease?O Fletcher, A M Kessling
Lancet (London, England)|August 31, 1985
Interpretation of presence of S2 alleleA M Kessling, S E Humphries
Clinical Genetics|October 1, 1985
A study of DNA polymorphisms around the human apolipoprotein AI gene in hyperlipidaemic and normal individualsA M Kessling, B Horsthemke, S E Humphries
Atherosclerosis|January 5, 1996
Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a 'null' LDL-receptor gene defectC Bétard, A M Kessling, M Roy, et al.
British Journal of Urology|November 7, 1998
Genetic initiation, progression and prognostic markers in transitional cell carcinoma of the bladder: a summary of the structural and transcriptional changes, and the role of developmental genesJ M Adshead, A M Kessling, C W Ogden
Ciba Foundation Symposium|January 1, 1987
Use of DNA polymorphisms of the apolipoprotein genes to study the role of genetic variation in the determination of serum lipid levelsS E Humphries, P J Talmud, A M Kessling
Clinical Genetics|June 1, 1986
DNA polymorphisms around the apo AI gene in normal and hyperlipidaemic individuals selected for a twin studyA M Kessling, K Berg, E Mockleby, et al.
Genomics|May 18, 1999
Novel methodology for the detection of chromosome 21-specific alpha-satellite DNA sequencesK Maratou, Y Siddique, A M Kessling, et al.
Human Genetics|July 29, 2000
Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunctionK Maratou, Y Siddique, A M Kessling, et al.
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