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Genetic testing

Showing results (261-270 of 679) with videos related to

Pageof 68
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Genetic Testing|September 12, 2001
Familial dysautonomia and the expansion of the Ashkenazi Jewish carrier screening panelF Gilbert
Genetic Testing|February 26, 2008
Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing lossRené Utrera, Vanessa Ridaura, Yuryanni Rodríguez, et al.
Genetic Testing|February 26, 2008
A novel mutation in the EXT2 gene identified in two unrelated Chinese families with hereditary multiple exostosesShi Guo Liu, Fei Feng Li, Shang Zhi Huang, et al.
Genetic Testing|February 26, 2008
Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolatesSonja Bouwer, Dora Angelicheva, David Chandler, et al.
Genetic Testing|April 15, 2008
Molecular genetic testing in the United States: comparison with international practiceMargaret M McGovern, Rob Elles, Elettra Ronchi, et al.
Genetic Testing|February 24, 2001
Disclosure of Huntington's disease to family members: the dilemma of known but unknowing partiesR Hakimian
Genetic Testing|February 24, 2001
Characterization of a novel D1S80 pseudoalleleE Mar, I Medintz, R Reynolds, et al.
Genetic Testing|January 6, 2001
Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinosesN A Zhong, K E Wisniewski, W Ju, et al.
Genetic Testing|January 6, 2001
FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardationM V Mulatinho, J C Llerena, M M Pimentel
Genetic Testing|January 6, 2001
Automated, PCR-RFLP genotyping of the urokinase geneS M Sell, F Blasi, F Booyse
Pageof 68

Showing results (261-270 of 679) with videos related to

Sort By:
Pageof 68
Genetic Testing|September 12, 2001
Familial dysautonomia and the expansion of the Ashkenazi Jewish carrier screening panelF Gilbert
Genetic Testing|February 26, 2008
Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing lossRené Utrera, Vanessa Ridaura, Yuryanni Rodríguez, et al.
Genetic Testing|February 26, 2008
A novel mutation in the EXT2 gene identified in two unrelated Chinese families with hereditary multiple exostosesShi Guo Liu, Fei Feng Li, Shang Zhi Huang, et al.
Genetic Testing|February 26, 2008
Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolatesSonja Bouwer, Dora Angelicheva, David Chandler, et al.
Genetic Testing|April 15, 2008
Molecular genetic testing in the United States: comparison with international practiceMargaret M McGovern, Rob Elles, Elettra Ronchi, et al.
Genetic Testing|February 24, 2001
Disclosure of Huntington's disease to family members: the dilemma of known but unknowing partiesR Hakimian
Genetic Testing|February 24, 2001
Characterization of a novel D1S80 pseudoalleleE Mar, I Medintz, R Reynolds, et al.
Genetic Testing|January 6, 2001
Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinosesN A Zhong, K E Wisniewski, W Ju, et al.
Genetic Testing|January 6, 2001
FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardationM V Mulatinho, J C Llerena, M M Pimentel
Genetic Testing|January 6, 2001
Automated, PCR-RFLP genotyping of the urokinase geneS M Sell, F Blasi, F Booyse
Pageof 68