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H Sobol

Showing results (31-40 of 94) with videos related to

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Oncogene|April 1, 1994
Two germ-line mutations affecting the same nucleotide at codon 257 of p53 gene, a rare site for mutationsS Mazoyer, P Lalle, C Moyret-Lalle, et al.
Revue Neurologique|January 1, 1991
[Genetics of neurofibromatosis: recent progress and prospects]M Maillet-Vioud, S Narod, D Assouline, et al.
International Journal of Oncology|May 6, 2011
Cumulative regional allelotyping of human breast carcinomasF Kerangueven, F Eisinger, F Allione, et al.
Oncology Reports|May 20, 2011
Multiple sites of loss of heterozygosity on chromosome arms 3p and 3q in human breast carcinomasF Kerangueven, T Noguchi, V Wargniez, et al.
Pediatrie|January 1, 1992
[Retinoblastoma]E Bouffet, D Frappaz, J D Grange, et al.
American Journal of Human Genetics|September 1, 1992
Genetic analysis of 24 French families with multiple endocrine neoplasia type 2AS A Narod, M F Lavoué, K Morgan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1994
[Constitutional translocation t(1;6) and Burkitt's lymphoma]C Berger, D Frappaz, E Bouffet, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1996
[Screening practices and familial antecedents of colorectal cancer. Survey with a voluntary population]F Eisinger, J P Giordanella, R Didelot, et al.
Bulletin Du Cancer|September 1, 1996
[Attitudes towards screening and prevention of breast and ovarian cancers with hereditary predisposition. Survey by female gynecologists in the north of France]P Vennin, S Giard, C Julian-Reynier, et al.
American Journal of Medical Genetics|September 12, 2000
Disclosure to the family of breast/ovarian cancer genetic test results: patient's willingness and associated factorsC Julian-Reynier, F Eisinger, F Chabal, et al.
Pageof 10

Showing results (31-40 of 94) with videos related to

Sort By:
Pageof 10
Oncogene|April 1, 1994
Two germ-line mutations affecting the same nucleotide at codon 257 of p53 gene, a rare site for mutationsS Mazoyer, P Lalle, C Moyret-Lalle, et al.
Revue Neurologique|January 1, 1991
[Genetics of neurofibromatosis: recent progress and prospects]M Maillet-Vioud, S Narod, D Assouline, et al.
International Journal of Oncology|May 6, 2011
Cumulative regional allelotyping of human breast carcinomasF Kerangueven, F Eisinger, F Allione, et al.
Oncology Reports|May 20, 2011
Multiple sites of loss of heterozygosity on chromosome arms 3p and 3q in human breast carcinomasF Kerangueven, T Noguchi, V Wargniez, et al.
Pediatrie|January 1, 1992
[Retinoblastoma]E Bouffet, D Frappaz, J D Grange, et al.
American Journal of Human Genetics|September 1, 1992
Genetic analysis of 24 French families with multiple endocrine neoplasia type 2AS A Narod, M F Lavoué, K Morgan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1994
[Constitutional translocation t(1;6) and Burkitt's lymphoma]C Berger, D Frappaz, E Bouffet, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1996
[Screening practices and familial antecedents of colorectal cancer. Survey with a voluntary population]F Eisinger, J P Giordanella, R Didelot, et al.
Bulletin Du Cancer|September 1, 1996
[Attitudes towards screening and prevention of breast and ovarian cancers with hereditary predisposition. Survey by female gynecologists in the north of France]P Vennin, S Giard, C Julian-Reynier, et al.
American Journal of Medical Genetics|September 12, 2000
Disclosure to the family of breast/ovarian cancer genetic test results: patient's willingness and associated factorsC Julian-Reynier, F Eisinger, F Chabal, et al.
Pageof 10