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Human genetics

Showing results (781-790 of 9,569) with videos related to

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Human Genetics|September 15, 2000
Genetic contribution of the BAT2 gene microsatellite polymorphism to the age-at-onset of insulin-dependent diabetes mellitusM Hashimoto, N Nakamura, H Obayashi, et al.
Human Genetics|September 15, 2000
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypesJ Balciuniene, N Dahl, P Jalonen, et al.
Human Genetics|September 15, 2000
Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentationJ Del-Favero, D Goossens, P De Jonghe, et al.
Human Genetics|September 15, 2000
DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patientsR A Perrichot, B Mercier, P M Simon, et al.
Human Genetics|September 15, 2000
Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndromeC A Joyce, A Sharp, J M Walker, et al.
Human Genetics|December 29, 2000
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failureA Marozzi, E Manfredini, M G Tibiletti, et al.
Human Genetics|December 29, 2000
Molecular analysis of the genotype-phenotype relationship in factor VII deficiencyD S Millar, G Kemball-Cook, J H McVey, et al.
Human Genetics|December 29, 2000
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancerJ T Bergthorsson, G Johannesdottir, A Arason, et al.
Human Genetics|December 29, 2000
Gene rearranagement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion geneN Tayebi, J Park, V Madike, et al.
Human Genetics|December 22, 1999
Mapping of a gene for May-Hegglin anomaly to chromosome 22qS Kunishima, T Kojima, T Tanaka, et al.
Pageof 957

Showing results (781-790 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|September 15, 2000
Genetic contribution of the BAT2 gene microsatellite polymorphism to the age-at-onset of insulin-dependent diabetes mellitusM Hashimoto, N Nakamura, H Obayashi, et al.
Human Genetics|September 15, 2000
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypesJ Balciuniene, N Dahl, P Jalonen, et al.
Human Genetics|September 15, 2000
Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentationJ Del-Favero, D Goossens, P De Jonghe, et al.
Human Genetics|September 15, 2000
DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patientsR A Perrichot, B Mercier, P M Simon, et al.
Human Genetics|September 15, 2000
Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndromeC A Joyce, A Sharp, J M Walker, et al.
Human Genetics|December 29, 2000
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failureA Marozzi, E Manfredini, M G Tibiletti, et al.
Human Genetics|December 29, 2000
Molecular analysis of the genotype-phenotype relationship in factor VII deficiencyD S Millar, G Kemball-Cook, J H McVey, et al.
Human Genetics|December 29, 2000
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancerJ T Bergthorsson, G Johannesdottir, A Arason, et al.
Human Genetics|December 29, 2000
Gene rearranagement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion geneN Tayebi, J Park, V Madike, et al.
Human Genetics|December 22, 1999
Mapping of a gene for May-Hegglin anomaly to chromosome 22qS Kunishima, T Kojima, T Tanaka, et al.
Pageof 957