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M Buraczynska

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American Journal of Human Genetics|November 1, 1985
Apolipoprotein A-I gene polymorphism and susceptibility of non-insulin-dependent diabetes mellitusM Buraczynska, J Hanzlik, M Grzywa
Human Genetics|October 1, 1986
ApoA-I related DNA polymorphism in humans with coronary heart diseaseM Buraczynska, J Hanzlik, M Grzywa
The American Journal of Tropical Medicine and Hygiene|September 1, 1980
Site-specific recombination in bacteriophage lambda: structural analyses of reactive DNA sequencesA Landy, P L Hsu, W Ross, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 6, 1998
A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosaG A Fishman, S Grover, M Buraczynska, et al.
Klinische Wochenschrift|July 15, 1987
Alpha 1-antitrypsin gene polymorphism related to respiratory system diseaseM Buraczynska, D Schött, A J Hanzlik, et al.
American Journal of Ophthalmology|July 1, 1997
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR geneS Andréasson, V Ponjavic, M Abrahamson, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Construction of human embryonic cDNA libraries: HD, PKD1 and BRCA1 are transcribed widely during embryogenesisM J Buraczynska, M L Van Keuren, K M Buraczynska, et al.
Ophthalmology|December 17, 1998
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Phenotype of an X-linked retinitis pigmentosa family with a novel splice defect in the RPGR geneS Bauer, R Fujita, M Buraczynska, et al.
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|November 1, 1985
Apolipoprotein A-I gene polymorphism and susceptibility of non-insulin-dependent diabetes mellitusM Buraczynska, J Hanzlik, M Grzywa
Human Genetics|October 1, 1986
ApoA-I related DNA polymorphism in humans with coronary heart diseaseM Buraczynska, J Hanzlik, M Grzywa
The American Journal of Tropical Medicine and Hygiene|September 1, 1980
Site-specific recombination in bacteriophage lambda: structural analyses of reactive DNA sequencesA Landy, P L Hsu, W Ross, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 6, 1998
A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosaG A Fishman, S Grover, M Buraczynska, et al.
Klinische Wochenschrift|July 15, 1987
Alpha 1-antitrypsin gene polymorphism related to respiratory system diseaseM Buraczynska, D Schött, A J Hanzlik, et al.
American Journal of Ophthalmology|July 1, 1997
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR geneS Andréasson, V Ponjavic, M Abrahamson, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Construction of human embryonic cDNA libraries: HD, PKD1 and BRCA1 are transcribed widely during embryogenesisM J Buraczynska, M L Van Keuren, K M Buraczynska, et al.
Ophthalmology|December 17, 1998
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Phenotype of an X-linked retinitis pigmentosa family with a novel splice defect in the RPGR geneS Bauer, R Fujita, M Buraczynska, et al.
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.
Pageof 2