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P Sistonen

Showing results (91-100 of 110) with videos related to

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Science (New York, N.Y.)|May 7, 1993
Genetic mapping of a locus predisposing to human colorectal cancerP Peltomäki, L A Aaltonen, P Sistonen, et al.
American Journal of Human Genetics|June 1, 1996
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21qK Virtaneva, J Miao, A L Träskelin, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Founder effect in spinal and bulbar muscular atrophy (SBMA) in ScandinaviaA Lund, B Udd, V Juvonen, et al.
Human Genetics|February 1, 1995
Genetic homogeneity of cartilage-hair hypoplasiaT Sulisalo, I van der Burgt, D L Rimoin, et al.
Nature Genetics|January 1, 1997
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysisA Hemminki, I Tomlinson, D Markie, et al.
Tissue Antigens|October 23, 2009
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populationsL L E Koskinen, E Einarsdottir, I R Korponay-Szabo, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Cell|September 22, 1995
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failureK Aittomäki, J L Lucena, P Pakarinen, et al.
Science (New York, N.Y.)|June 6, 1998
Mutations in the SMAD4/DPC4 gene in juvenile polyposisJ R Howe, S Roth, J C Ringold, et al.
Genes, Chromosomes & Cancer|August 10, 1999
SMAD genes in juvenile polyposisS Roth, P Sistonen, R Salovaara, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
Science (New York, N.Y.)|May 7, 1993
Genetic mapping of a locus predisposing to human colorectal cancerP Peltomäki, L A Aaltonen, P Sistonen, et al.
American Journal of Human Genetics|June 1, 1996
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21qK Virtaneva, J Miao, A L Träskelin, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Founder effect in spinal and bulbar muscular atrophy (SBMA) in ScandinaviaA Lund, B Udd, V Juvonen, et al.
Human Genetics|February 1, 1995
Genetic homogeneity of cartilage-hair hypoplasiaT Sulisalo, I van der Burgt, D L Rimoin, et al.
Nature Genetics|January 1, 1997
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysisA Hemminki, I Tomlinson, D Markie, et al.
Tissue Antigens|October 23, 2009
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populationsL L E Koskinen, E Einarsdottir, I R Korponay-Szabo, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Cell|September 22, 1995
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failureK Aittomäki, J L Lucena, P Pakarinen, et al.
Science (New York, N.Y.)|June 6, 1998
Mutations in the SMAD4/DPC4 gene in juvenile polyposisJ R Howe, S Roth, J C Ringold, et al.
Genes, Chromosomes & Cancer|August 10, 1999
SMAD genes in juvenile polyposisS Roth, P Sistonen, R Salovaara, et al.
Pageof 11