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P Sistonen

Showing results (61-70 of 110) with videos related to

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Forensic Science International|September 16, 1994
A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicineA Sajantila, P Pacek, M Lukka, et al.
Human Molecular Genetics|August 1, 1993
Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mappingA E Lehesjoki, M Koskiniemi, R Norio, et al.
Genomics|December 15, 1996
Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous regionT Joensuu, G Blanco, L Pakarinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1994
[Linkage and linkage disequilibrium in the Finnish disease heritage]A de la Chapelle, J Hästbacka, A E Lehesjoki, et al.
Human Mutation|February 12, 2000
A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. OnlineM Wolf, A Hemminki, A Kivioja, et al.
Genomics|March 20, 1995
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysisE Tahvanainen, H Forsius, E Karila, et al.
Genomics|December 10, 1995
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2E Tahvanainen, H Forsius, M Damsten, et al.
Blood|August 15, 2000
Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in FinnsF Sidoux-Walter, N Lucien, R Nissinen, et al.
Vox Sanguinis|May 1, 1981
Nea, new blood group antigen in FinlandP Sistonen, H R Nevanlinna, K Virtaranta-Knowles, et al.
Genomics|September 1, 1992
Mapping of the regulatory subunits RI beta and RII beta of cAMP-dependent protein kinase genes on human chromosome 7R Solberg, P Sistonen, A L Träskelin, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Forensic Science International|September 16, 1994
A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicineA Sajantila, P Pacek, M Lukka, et al.
Human Molecular Genetics|August 1, 1993
Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mappingA E Lehesjoki, M Koskiniemi, R Norio, et al.
Genomics|December 15, 1996
Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous regionT Joensuu, G Blanco, L Pakarinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1994
[Linkage and linkage disequilibrium in the Finnish disease heritage]A de la Chapelle, J Hästbacka, A E Lehesjoki, et al.
Human Mutation|February 12, 2000
A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. OnlineM Wolf, A Hemminki, A Kivioja, et al.
Genomics|March 20, 1995
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysisE Tahvanainen, H Forsius, E Karila, et al.
Genomics|December 10, 1995
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2E Tahvanainen, H Forsius, M Damsten, et al.
Blood|August 15, 2000
Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in FinnsF Sidoux-Walter, N Lucien, R Nissinen, et al.
Vox Sanguinis|May 1, 1981
Nea, new blood group antigen in FinlandP Sistonen, H R Nevanlinna, K Virtaranta-Knowles, et al.
Genomics|September 1, 1992
Mapping of the regulatory subunits RI beta and RII beta of cAMP-dependent protein kinase genes on human chromosome 7R Solberg, P Sistonen, A L Träskelin, et al.
Pageof 11