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H Sobol

Showing results (51-60 of 94) with videos related to

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Cancer Research|February 1, 1996
Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancerF Eisinger, D Stoppa-Lyonnet, M Longy, et al.
European Journal of Cancer (Oxford, England : 1990)|January 20, 1999
Cancer genetic clinics: why do women who already have cancer attend?C Julian-Reynier, F Eisinger, F Chabal, et al.
Oncology Reports|June 19, 1998
Time elapsing from cancer diagnosis and anxiety in women attending cancer genetic clinicsC Julian-Reynier, F Eisinger, F Chabal, et al.
International Journal of Oncology|May 11, 2011
Analyses of linkage to 17q11-q23 in 3 French hereditary nonpolyposis colon-cancer familiesD Bernardgallon, S Gosse, L Essioux, et al.
Presse Medicale (Paris, France : 1983)|March 31, 1990
[Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families]C Houdent, B Avronsart, M Dubuisson, et al.
International Journal of Cancer|August 17, 1999
Histological type and syncytial growth pattern affect E-cadherin expression in a multifactorial analysis of a combined panel of sporadic and BRCA1-associated breast cancersJ Jacquemier, F Eisinger, C Noguès, et al.
Genomics|August 1, 1989
Linked markers flanking the gene for multiple endocrine neoplasia type 2AY Nakamura, C G Mathew, H Sobol, et al.
Cancer Research|January 4, 1998
Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomasF Kerangueven, T Noguchi, F Coulier, et al.
Cancer Genetics and Cytogenetics|November 11, 1998
Constitutional balanced pericentric inversions of chromosomes X, 2, and 5 in myeloid malignanciesM J Mozziconacci, H Sobol, N Philip, et al.
The New England Journal of Medicine|October 12, 1989
Screening for multiple endocrine neoplasia type 2a with DNA-polymorphism analysisH Sobol, S A Narod, Y Nakamura, et al.
Pageof 10

Showing results (51-60 of 94) with videos related to

Sort By:
Pageof 10
Cancer Research|February 1, 1996
Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancerF Eisinger, D Stoppa-Lyonnet, M Longy, et al.
European Journal of Cancer (Oxford, England : 1990)|January 20, 1999
Cancer genetic clinics: why do women who already have cancer attend?C Julian-Reynier, F Eisinger, F Chabal, et al.
Oncology Reports|June 19, 1998
Time elapsing from cancer diagnosis and anxiety in women attending cancer genetic clinicsC Julian-Reynier, F Eisinger, F Chabal, et al.
International Journal of Oncology|May 11, 2011
Analyses of linkage to 17q11-q23 in 3 French hereditary nonpolyposis colon-cancer familiesD Bernardgallon, S Gosse, L Essioux, et al.
Presse Medicale (Paris, France : 1983)|March 31, 1990
[Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families]C Houdent, B Avronsart, M Dubuisson, et al.
International Journal of Cancer|August 17, 1999
Histological type and syncytial growth pattern affect E-cadherin expression in a multifactorial analysis of a combined panel of sporadic and BRCA1-associated breast cancersJ Jacquemier, F Eisinger, C Noguès, et al.
Genomics|August 1, 1989
Linked markers flanking the gene for multiple endocrine neoplasia type 2AY Nakamura, C G Mathew, H Sobol, et al.
Cancer Research|January 4, 1998
Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomasF Kerangueven, T Noguchi, F Coulier, et al.
Cancer Genetics and Cytogenetics|November 11, 1998
Constitutional balanced pericentric inversions of chromosomes X, 2, and 5 in myeloid malignanciesM J Mozziconacci, H Sobol, N Philip, et al.
The New England Journal of Medicine|October 12, 1989
Screening for multiple endocrine neoplasia type 2a with DNA-polymorphism analysisH Sobol, S A Narod, Y Nakamura, et al.
Pageof 10