Search research articles
Contact Us
Filters
Showing results (61-70 of 94) with videos related to
Page
of 10
Sort By:
Bulletin Du Cancer
|
February 1, 1993
Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysis
H Sobol, S Mazoyer, S A Smith, et al.
Human Genetics
|
June 1, 1992
Genetic heterogeneity of early-onset familial breast cancer
H 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 regions
F 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 syndrome
A Imbert, M Chaffanet, L Essioux, et al.
Human Genetics
|
November 1, 1989
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma
S 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 recruitment
F 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 line
J 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 features
F Eisinger, C Noguès, J M Guinebretière, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 94) with videos related to
Sort By:
Page
of 10
Bulletin Du Cancer
|
February 1, 1993
Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysis
H Sobol, S Mazoyer, S A Smith, et al.
Human Genetics
|
June 1, 1992
Genetic heterogeneity of early-onset familial breast cancer
H 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 regions
F 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 syndrome
A Imbert, M Chaffanet, L Essioux, et al.
Human Genetics
|
November 1, 1989
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma
S 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 recruitment
F 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 line
J 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 features
F Eisinger, C Noguès, J M Guinebretière, et al.
Page
of 10