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C T Falk

Showing results (31-40 of 46) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1974
Proceedings: A possible gene assignment to chromosome 21L Jackson, C T Falk, F H Allen, et al.
Genetic Epidemiology|January 1, 1995
Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methodsC T Falk, A Ashley, N Lamb, et al.
American Journal of Human Genetics|March 1, 1986
Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfectaC T Falk, R C Schwartz, F Ramirez, et al.
Series Haematologica (1968)|January 11, 1975
Autosomal linkage in humans (methodology and results of computer analysis)C T Falk, M E Walker, M D Martin, et al.
Genetic Epidemiology|January 1, 1984
Genetic Analysis Workshop II: summaryJ W MacCluer, C T Falk, R S Spielman, et al.
American Journal of Human Genetics|June 13, 1998
Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophyC T Falk, J M Gilchrist, M A Pericak-Vance, et al.
Humangenetik|June 26, 1974
Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traitsJ L Simpson, C T Falk, G Morillo-Cucci, et al.
Genetic Epidemiology|December 22, 1999
Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and whyD A Greenberg, J W MacCluer, M A Spence, et al.
Advances in Neurology|January 1, 1988
Linkage studies in families with dystonia: linkage analysis as a tool to locate and characterize the gene(s) for dystoniaC T Falk, S B Bressman, F H Allen, et al.
Genomics|August 1, 1996
Physical mapping of a commonly deleted region, the site of a candidate tumor suppressor gene, at 12q22 in human male germ cell tumorsV V Murty, B Renault, C T Falk, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Cytogenetics and Cell Genetics|January 1, 1974
Proceedings: A possible gene assignment to chromosome 21L Jackson, C T Falk, F H Allen, et al.
Genetic Epidemiology|January 1, 1995
Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methodsC T Falk, A Ashley, N Lamb, et al.
American Journal of Human Genetics|March 1, 1986
Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfectaC T Falk, R C Schwartz, F Ramirez, et al.
Series Haematologica (1968)|January 11, 1975
Autosomal linkage in humans (methodology and results of computer analysis)C T Falk, M E Walker, M D Martin, et al.
Genetic Epidemiology|January 1, 1984
Genetic Analysis Workshop II: summaryJ W MacCluer, C T Falk, R S Spielman, et al.
American Journal of Human Genetics|June 13, 1998
Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophyC T Falk, J M Gilchrist, M A Pericak-Vance, et al.
Humangenetik|June 26, 1974
Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traitsJ L Simpson, C T Falk, G Morillo-Cucci, et al.
Genetic Epidemiology|December 22, 1999
Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and whyD A Greenberg, J W MacCluer, M A Spence, et al.
Advances in Neurology|January 1, 1988
Linkage studies in families with dystonia: linkage analysis as a tool to locate and characterize the gene(s) for dystoniaC T Falk, S B Bressman, F H Allen, et al.
Genomics|August 1, 1996
Physical mapping of a commonly deleted region, the site of a candidate tumor suppressor gene, at 12q22 in human male germ cell tumorsV V Murty, B Renault, C T Falk, et al.
Pageof 5