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P Tonin

Showing results (71-80 of 110) with videos related to

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American Journal of Human Genetics|January 1, 1996
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer familiesO Serova, M Montagna, D Torchard, et al.
Journal of Medical Genetics|December 1, 1995
A large multisite cancer family is linked to BRCA2P Tonin, P Ghadirian, C Phelan, et al.
Nature Genetics|December 1, 1994
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesJ Simard, P Tonin, F Durocher, et al.
Nature Genetics|August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21N Rahman, L Arbour, P Tonin, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathyG Vattemi, M Neri, S Piffer, et al.
Genomics|August 10, 1995
Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21J M Rommens, F Durocher, J McArthur, et al.
Human Molecular Genetics|August 1, 1993
Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12-21: exclusion of candidate genes EDH17B2 and RARAJ Simard, J Feunteun, G Lenoir, et al.
Clinical Genetics|July 17, 2001
Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancerP O Chappuis, N Hamel, A J Paradis, et al.
Genes, Chromosomes & Cancer|July 1, 1995
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage ConsortiumR S Cornelis, S L Neuhausen, O Johansson, et al.
Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.
Pageof 11

Showing results (71-80 of 110) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|January 1, 1996
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer familiesO Serova, M Montagna, D Torchard, et al.
Journal of Medical Genetics|December 1, 1995
A large multisite cancer family is linked to BRCA2P Tonin, P Ghadirian, C Phelan, et al.
Nature Genetics|December 1, 1994
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesJ Simard, P Tonin, F Durocher, et al.
Nature Genetics|August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21N Rahman, L Arbour, P Tonin, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathyG Vattemi, M Neri, S Piffer, et al.
Genomics|August 10, 1995
Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21J M Rommens, F Durocher, J McArthur, et al.
Human Molecular Genetics|August 1, 1993
Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12-21: exclusion of candidate genes EDH17B2 and RARAJ Simard, J Feunteun, G Lenoir, et al.
Clinical Genetics|July 17, 2001
Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancerP O Chappuis, N Hamel, A J Paradis, et al.
Genes, Chromosomes & Cancer|July 1, 1995
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage ConsortiumR S Cornelis, S L Neuhausen, O Johansson, et al.
Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.
Pageof 11