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P Sistonen

Showing results (51-60 of 110) with videos related to

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Transfusion|June 1, 1996
Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 allelesS Lee, X Wu, S Son, et al.
Nature Genetics|June 1, 1994
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysisE Tahvanainen, R Norio, E Karila, et al.
Nature Genetics|April 1, 1993
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysisT Sulisalo, P Sistonen, J Hästbacka, et al.
Blood|August 1, 1995
Molecular basis of the RhCW (Rh8) and RhCX (Rh9) blood group specificitiesI Mouro, Y Colin, P Sistonen, et al.
Human Molecular Genetics|January 1, 1995
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3qE M Sankila, L Pakarinen, H Kääriäinen, et al.
American Journal of Human Genetics|June 1, 1997
Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14T Lauteala, P Sistonen, M L Savontaus, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1991
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22A E Lehesjoki, M Koskiniemi, P Sistonen, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathyT Lamminen, K Huoponen, P Sistonen, et al.
Vox Sanguinis|January 1, 1987
WES, a 'new' infrequent blood group antigen in FinnsP Sistonen, H R Nevanlinna, K Virtaranta-Knowles, et al.
American Journal of Human Genetics|November 1, 1994
High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia geneT Sulisalo, J Klockars, O Mäkitie, et al.
Pageof 11

Showing results (51-60 of 110) with videos related to

Sort By:
Pageof 11
Transfusion|June 1, 1996
Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 allelesS Lee, X Wu, S Son, et al.
Nature Genetics|June 1, 1994
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysisE Tahvanainen, R Norio, E Karila, et al.
Nature Genetics|April 1, 1993
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysisT Sulisalo, P Sistonen, J Hästbacka, et al.
Blood|August 1, 1995
Molecular basis of the RhCW (Rh8) and RhCX (Rh9) blood group specificitiesI Mouro, Y Colin, P Sistonen, et al.
Human Molecular Genetics|January 1, 1995
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3qE M Sankila, L Pakarinen, H Kääriäinen, et al.
American Journal of Human Genetics|June 1, 1997
Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14T Lauteala, P Sistonen, M L Savontaus, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1991
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22A E Lehesjoki, M Koskiniemi, P Sistonen, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathyT Lamminen, K Huoponen, P Sistonen, et al.
Vox Sanguinis|January 1, 1987
WES, a 'new' infrequent blood group antigen in FinnsP Sistonen, H R Nevanlinna, K Virtaranta-Knowles, et al.
American Journal of Human Genetics|November 1, 1994
High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia geneT Sulisalo, J Klockars, O Mäkitie, et al.
Pageof 11