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Gene
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August 6, 1999
Genomic structure of the human PLZF gene
E M van Schothorst, D E Prins, B E Baysal, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes
E M van Schothorst, J C Jansen, A F Bardoel, et al.
American Journal of Human Genetics
|
March 21, 2000
ATM-heterozygous germline mutations contribute to breast cancer-susceptibility
A Broeks, J H Urbanus, A N Floore, et al.
Genes, Chromosomes & Cancer
|
June 8, 2001
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
P E Taschner, J C Jansen, B E Baysal, et al.
Cancer Research
|
August 1, 1994
Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations
R S Cornelis, M van Vliet, C B Vos, et al.
European Journal of Human Genetics : EJHG
|
July 21, 2001
Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testing
L Lodder, P G Frets, R W Trijsburg, et al.
Lancet (London, England)
|
July 8, 2000
Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation
E J Meijers-Heijboer, L C Verhoog, C T Brekelmans, et al.
Journal of Medical Genetics
|
February 27, 2004
Extending the p16-Leiden tumour spectrum by respiratory tract tumours
R A Oldenburg, W H de Vos tot Nederveen Cappel, M van Puijenbroek, et al.
British Journal of Cancer
|
June 12, 2014
Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy
M Kriege, A Hollestelle, A Jager, et al.
Journal of Medical Genetics
|
December 14, 1999
Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks? Rotterdam/Leiden Genetics Working Group
L N Lodder, P G Frets, R W Trijsburg, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 119) with videos related to
Sort By:
Page
of 12
Gene
|
August 6, 1999
Genomic structure of the human PLZF gene
E M van Schothorst, D E Prins, B E Baysal, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes
E M van Schothorst, J C Jansen, A F Bardoel, et al.
American Journal of Human Genetics
|
March 21, 2000
ATM-heterozygous germline mutations contribute to breast cancer-susceptibility
A Broeks, J H Urbanus, A N Floore, et al.
Genes, Chromosomes & Cancer
|
June 8, 2001
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
P E Taschner, J C Jansen, B E Baysal, et al.
Cancer Research
|
August 1, 1994
Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations
R S Cornelis, M van Vliet, C B Vos, et al.
European Journal of Human Genetics : EJHG
|
July 21, 2001
Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testing
L Lodder, P G Frets, R W Trijsburg, et al.
Lancet (London, England)
|
July 8, 2000
Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation
E J Meijers-Heijboer, L C Verhoog, C T Brekelmans, et al.
Journal of Medical Genetics
|
February 27, 2004
Extending the p16-Leiden tumour spectrum by respiratory tract tumours
R A Oldenburg, W H de Vos tot Nederveen Cappel, M van Puijenbroek, et al.
British Journal of Cancer
|
June 12, 2014
Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy
M Kriege, A Hollestelle, A Jager, et al.
Journal of Medical Genetics
|
December 14, 1999
Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks? Rotterdam/Leiden Genetics Working Group
L N Lodder, P G Frets, R W Trijsburg, et al.
Page
of 12