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R Varon

Showing results (31-40 of 36) with videos related to

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Human Genetics|May 1, 1997
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survivalM Macek, M Macek, A Krebsová, et al.
Journal of Computational Chemistry|October 21, 2010
Computerized evaluation of mean residence times in multicompartmental linear system and pharmacokineticsJ M Villalba, A J Barbero, R Diaz-Sierra, et al.
Molecular Cell|January 10, 2002
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiencyM O'Driscoll, K M Cerosaletti, P M Girard, et al.
Cell|May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.
British Journal of Cancer|June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter studyA Jakubowska, D Rozkrut, A Antoniou, et al.
British Journal of Cancer|November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)A Osorio, R L Milne, G Pita, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Human Genetics|May 1, 1997
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survivalM Macek, M Macek, A Krebsová, et al.
Journal of Computational Chemistry|October 21, 2010
Computerized evaluation of mean residence times in multicompartmental linear system and pharmacokineticsJ M Villalba, A J Barbero, R Diaz-Sierra, et al.
Molecular Cell|January 10, 2002
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiencyM O'Driscoll, K M Cerosaletti, P M Girard, et al.
Cell|May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.
British Journal of Cancer|June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter studyA Jakubowska, D Rozkrut, A Antoniou, et al.
British Journal of Cancer|November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)A Osorio, R L Milne, G Pita, et al.
Pageof 4