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S Kamakari

Showing results (1-10 of 14) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1995
FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal XpS Kamakari, D Thiselton, S Lindsay, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Assignment of a human cold shock domain protein A intronless pseudogene (CSDAP1) to human chromosome 16 band p11.2 by in situ hybridizationA Argyrokastritis, J Kontaraki, S Kamakari, et al.
Human Genetics|February 1, 1997
Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17A Argyrokastritis, S Kamakari, M Kapsetaki, et al.
Human Molecular Genetics|December 1, 1992
Dinucleotide repeat polymorphism at the DXS559 locusP Roustan, A R Curtis, S Kamakari, et al.
Human Molecular Genetics|January 1, 1993
Dinucleotide repeat polymorphism at the DXS573 locusP Roustan, A R Curtis, S Kamakari, et al.
Human Molecular Genetics|December 1, 1992
Two dinucleotide repeat polymorphisms at the DXS571 locusA R Curtis, P Roustan, S Kamakari, et al.
Genomics|October 1, 1992
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13)M E Porteous, A Curtis, S Lindsay, et al.
Genomics|January 1, 1995
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22D L Thiselton, S Lindsay, S Kamakari, et al.
Genomics|July 1, 1993
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosomeS Lindsay, A R Curtis, P Roustan, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at the DXS556 locusD L Thiselton, S Kamakari, A R Curtis, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Cytogenetics and Cell Genetics|January 1, 1995
FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal XpS Kamakari, D Thiselton, S Lindsay, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Assignment of a human cold shock domain protein A intronless pseudogene (CSDAP1) to human chromosome 16 band p11.2 by in situ hybridizationA Argyrokastritis, J Kontaraki, S Kamakari, et al.
Human Genetics|February 1, 1997
Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17A Argyrokastritis, S Kamakari, M Kapsetaki, et al.
Human Molecular Genetics|December 1, 1992
Dinucleotide repeat polymorphism at the DXS559 locusP Roustan, A R Curtis, S Kamakari, et al.
Human Molecular Genetics|January 1, 1993
Dinucleotide repeat polymorphism at the DXS573 locusP Roustan, A R Curtis, S Kamakari, et al.
Human Molecular Genetics|December 1, 1992
Two dinucleotide repeat polymorphisms at the DXS571 locusA R Curtis, P Roustan, S Kamakari, et al.
Genomics|October 1, 1992
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13)M E Porteous, A Curtis, S Lindsay, et al.
Genomics|January 1, 1995
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22D L Thiselton, S Lindsay, S Kamakari, et al.
Genomics|July 1, 1993
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosomeS Lindsay, A R Curtis, P Roustan, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at the DXS556 locusD L Thiselton, S Kamakari, A R Curtis, et al.
Pageof 2