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Genetic testing

Showing results (121-130 of 679) with videos related to

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Genetic Testing|April 19, 2002
A primer for predicting risk of disease in HFE-linked hemochromatosisP C Adams, A P Walker, R T Acton
Genetic Testing|April 19, 2002
Acceptance of neonatal genetic screening for hereditary hemochromatosis by informed parentsM Bassett, C Dunn, K Battese, et al.
Genetic Testing|April 19, 2002
Mutation analysis in Rett syndromeJ M Milunsky, R V Lebo, T Ikuta, et al.
Genetic Testing|April 19, 2002
Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneityE Levy-Nissenbaum, M Eldar, Q Wang, et al.
Genetic Testing|December 29, 2005
LARaLink 2.0: a comprehensive aid to basic and clinical cytogenetic researchAdrian E Platts, Julie S Moldenhauer, Brian Fayz, et al.
Genetic Testing|July 26, 2008
Absence of H186R polymorphism in exon 4 of the APOBEC3G gene among North Indian individualsAnurag Rathore, Animesh Chatterjee, Naohiko Yamamoto, et al.
Genetic Testing|August 1, 2008
Explaining behavior change after genetic testing: the problem of collinearity between test results and risk estimatesThomas R Fanshawe, A Toby Prevost, J Scott Roberts, et al.
Genetic Testing|August 1, 2008
A novel mutation in EXT2 gene in a Chinese family with hereditary multiple exostosesShi Guo Liu, De Guo Lu, Zhong Qiang Liu, et al.
Genetic Testing|December 17, 2008
Co-occurrence of sporadic parkinsonism and late-onset Alzheimer's disease in a Brazilian male with the LRRK2 p.G2019S mutationCíntia B Santos-Rebouças, Cláudia B Abdalla, Fábio José R Baldi, et al.
Genetic Testing|December 17, 2008
Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan populationOmar Abidi, Redouane Boulouiz, Halima Nahili, et al.
Pageof 68

Showing results (121-130 of 679) with videos related to

Sort By:
Pageof 68
Genetic Testing|April 19, 2002
A primer for predicting risk of disease in HFE-linked hemochromatosisP C Adams, A P Walker, R T Acton
Genetic Testing|April 19, 2002
Acceptance of neonatal genetic screening for hereditary hemochromatosis by informed parentsM Bassett, C Dunn, K Battese, et al.
Genetic Testing|April 19, 2002
Mutation analysis in Rett syndromeJ M Milunsky, R V Lebo, T Ikuta, et al.
Genetic Testing|April 19, 2002
Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneityE Levy-Nissenbaum, M Eldar, Q Wang, et al.
Genetic Testing|December 29, 2005
LARaLink 2.0: a comprehensive aid to basic and clinical cytogenetic researchAdrian E Platts, Julie S Moldenhauer, Brian Fayz, et al.
Genetic Testing|July 26, 2008
Absence of H186R polymorphism in exon 4 of the APOBEC3G gene among North Indian individualsAnurag Rathore, Animesh Chatterjee, Naohiko Yamamoto, et al.
Genetic Testing|August 1, 2008
Explaining behavior change after genetic testing: the problem of collinearity between test results and risk estimatesThomas R Fanshawe, A Toby Prevost, J Scott Roberts, et al.
Genetic Testing|August 1, 2008
A novel mutation in EXT2 gene in a Chinese family with hereditary multiple exostosesShi Guo Liu, De Guo Lu, Zhong Qiang Liu, et al.
Genetic Testing|December 17, 2008
Co-occurrence of sporadic parkinsonism and late-onset Alzheimer's disease in a Brazilian male with the LRRK2 p.G2019S mutationCíntia B Santos-Rebouças, Cláudia B Abdalla, Fábio José R Baldi, et al.
Genetic Testing|December 17, 2008
Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan populationOmar Abidi, Redouane Boulouiz, Halima Nahili, et al.
Pageof 68