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H Sobol

Showing results (61-70 of 94) with videos related to

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Bulletin Du Cancer|February 1, 1993
Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysisH Sobol, S Mazoyer, S A Smith, et al.
Human Genetics|June 1, 1992
Genetic heterogeneity of early-onset familial breast cancerH Sobol, S Mazoyer, S A Narod, et al.
Oncogene|January 23, 1997
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regionsF Kerangueven, F Eisinger, T Noguchi, et al.
Genomics|February 15, 1996
Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndromeA Imbert, M Chaffanet, L Essioux, et al.
Human Genetics|November 1, 1989
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytomaS A Narod, H Sobol, Y Nakamura, et al.
La Revue De Medecine Interne|February 16, 2005
[HNPCC syndrome (hereditary non polyposis colon cancer): identification and management]S Olschwang, C Bonaïti, J Feingold, et al.
Familial Cancer|October 24, 2003
Cancer prone persons. A randomized screening trial based on colonoscopy: background, design and recruitmentF Eisinger, J P Giordanella, A Brigand, et al.
International Journal of Oncology|March 16, 2000
Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell lineJ Adélaïde, M Chaffanet, M J Mozziconacci, et al.
Pathologie-Biologie|May 9, 2006
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]S Olschwang, C Bonaïti-Pellié, J Feingold, et al.
International Journal of Cancer|June 17, 1999
Novel indications for BRCA1 screening using individual clinical and morphological featuresF Eisinger, C Noguès, J M Guinebretière, et al.
Pageof 10

Showing results (61-70 of 94) with videos related to

Sort By:
Pageof 10
Bulletin Du Cancer|February 1, 1993
Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysisH Sobol, S Mazoyer, S A Smith, et al.
Human Genetics|June 1, 1992
Genetic heterogeneity of early-onset familial breast cancerH Sobol, S Mazoyer, S A Narod, et al.
Oncogene|January 23, 1997
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regionsF Kerangueven, F Eisinger, T Noguchi, et al.
Genomics|February 15, 1996
Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndromeA Imbert, M Chaffanet, L Essioux, et al.
Human Genetics|November 1, 1989
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytomaS A Narod, H Sobol, Y Nakamura, et al.
La Revue De Medecine Interne|February 16, 2005
[HNPCC syndrome (hereditary non polyposis colon cancer): identification and management]S Olschwang, C Bonaïti, J Feingold, et al.
Familial Cancer|October 24, 2003
Cancer prone persons. A randomized screening trial based on colonoscopy: background, design and recruitmentF Eisinger, J P Giordanella, A Brigand, et al.
International Journal of Oncology|March 16, 2000
Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell lineJ Adélaïde, M Chaffanet, M J Mozziconacci, et al.
Pathologie-Biologie|May 9, 2006
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]S Olschwang, C Bonaïti-Pellié, J Feingold, et al.
International Journal of Cancer|June 17, 1999
Novel indications for BRCA1 screening using individual clinical and morphological featuresF Eisinger, C Noguès, J M Guinebretière, et al.
Pageof 10