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J M Connor

Showing results (131-140 of 181) with videos related to

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Lancet (London, England)|March 21, 1992
Fibrinogen genotype and risk of peripheral atherosclerosisF G Fowkes, J M Connor, F B Smith, et al.
Journal of Medical Genetics|July 1, 1992
Genetic variation at fibrinogen loci and plasma fibrinogen levelsJ M Connor, F G Fowkes, J Wood, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|January 1, 1995
Thrombocytopenia with absent radii (TAR) syndrome: a new increased cellular radiosensitivity syndromeR P Symonds, B J Clark, W D George, et al.
Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.
Journal of Medical Genetics|August 1, 1986
Application of three intragenic DNA polymorphisms for carrier detection in haemophilia BJ M Connor, A F Pettigrew, C Shiach, et al.
Atherosclerosis|April 27, 2000
Methylene tetrahydrofolate reductase (MTHFR) and nitric oxide synthase (ecNOS) genes and risks of peripheral arterial disease and coronary heart disease: Edinburgh Artery StudyF G Fowkes, A J Lee, C M Hau, et al.
Journal of Medical Genetics|March 1, 1993
Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1)M Nellist, P T Brook-Carter, J M Connor, et al.
Journal of Medical Genetics|April 16, 1998
A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardationS R Ghaffari, E Boyd, J L Tolmie, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
A fucosidosis patient with relative longevity and a missense mutation in exon 7 of the alpha-fucosidase geneC J Fleming, D U Sinclair, E J White, et al.
Journal of Medical Genetics|July 1, 1995
Detection of Y mosaicism in patients with Turner's syndromeC E Chu, J M Connor, M D Donaldson, et al.
Pageof 19

Showing results (131-140 of 181) with videos related to

Sort By:
Pageof 19
Lancet (London, England)|March 21, 1992
Fibrinogen genotype and risk of peripheral atherosclerosisF G Fowkes, J M Connor, F B Smith, et al.
Journal of Medical Genetics|July 1, 1992
Genetic variation at fibrinogen loci and plasma fibrinogen levelsJ M Connor, F G Fowkes, J Wood, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|January 1, 1995
Thrombocytopenia with absent radii (TAR) syndrome: a new increased cellular radiosensitivity syndromeR P Symonds, B J Clark, W D George, et al.
Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.
Journal of Medical Genetics|August 1, 1986
Application of three intragenic DNA polymorphisms for carrier detection in haemophilia BJ M Connor, A F Pettigrew, C Shiach, et al.
Atherosclerosis|April 27, 2000
Methylene tetrahydrofolate reductase (MTHFR) and nitric oxide synthase (ecNOS) genes and risks of peripheral arterial disease and coronary heart disease: Edinburgh Artery StudyF G Fowkes, A J Lee, C M Hau, et al.
Journal of Medical Genetics|March 1, 1993
Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1)M Nellist, P T Brook-Carter, J M Connor, et al.
Journal of Medical Genetics|April 16, 1998
A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardationS R Ghaffari, E Boyd, J L Tolmie, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
A fucosidosis patient with relative longevity and a missense mutation in exon 7 of the alpha-fucosidase geneC J Fleming, D U Sinclair, E J White, et al.
Journal of Medical Genetics|July 1, 1995
Detection of Y mosaicism in patients with Turner's syndromeC E Chu, J M Connor, M D Donaldson, et al.
Pageof 19