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Genetic testing

Showing results (441-450 of 679) with videos related to

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Genetic Testing|May 4, 2000
Identification of the Hind III polymorphic site in the PAI-1 gene: analysis of the PAI-1 Hind III polymorphism by PCRH E Grenett, N Khan, W Jiang, et al.
Genetic Testing|May 4, 2000
Evaluation of the prothrombin gene polymorphism in patients with advanced retinopathy of prematurityM Hiraoka, B S Shastry
Genetic Testing|February 24, 2001
Biallelic discrimination assays for the three common Ashkenazi Jewish mutations and a common non-Jewish mutation, in Tay-Sachs disease, using fluorogenic TaqMan probesC P Ward, A H Fensom, P M Green
Genetic Testing|September 25, 1999
The missing link in linkage analysis: the well sibling revisitedJ H Fanos
Genetic Testing|September 25, 1999
Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric communityK K Milner, T Han, E M Petty
Genetic Testing|September 25, 1999
A 6-year experience demonstrates the utility of screening for both cytogenetic and FMR-1 abnormalities in patients with mental retardationB J White, M Ayad, A Fraser, et al.
Genetic Testing|September 25, 1999
Prenatal diagnosis and the subsequent mutation analysis in a family with carbohydrate-deficient glycoprotein type I syndrome: growing evidence to support founder effects within CDG1 populationsA Crosby, S Jeffery, T Homfray, et al.
Genetic Testing|September 25, 1999
Disease genes and chromosomes: disease maps of the human genome. Chromosome 15F Gilbert
Genetic Testing|January 6, 2001
Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndromeJ Tzountzouris, D Kennedy, M Skuterud, et al.
Genetic Testing|January 6, 2001
Rapid mutation screening of phenylketonuria by polymerase chain reaction-linked restriction enzyme assay and direct sequence of the phenylalanine hydroxylase gene: clinical application in northern Japan and northern ChinaH Sueoka, M Nagao, S Chiba
Pageof 68

Showing results (441-450 of 679) with videos related to

Sort By:
Pageof 68
Genetic Testing|May 4, 2000
Identification of the Hind III polymorphic site in the PAI-1 gene: analysis of the PAI-1 Hind III polymorphism by PCRH E Grenett, N Khan, W Jiang, et al.
Genetic Testing|May 4, 2000
Evaluation of the prothrombin gene polymorphism in patients with advanced retinopathy of prematurityM Hiraoka, B S Shastry
Genetic Testing|February 24, 2001
Biallelic discrimination assays for the three common Ashkenazi Jewish mutations and a common non-Jewish mutation, in Tay-Sachs disease, using fluorogenic TaqMan probesC P Ward, A H Fensom, P M Green
Genetic Testing|September 25, 1999
The missing link in linkage analysis: the well sibling revisitedJ H Fanos
Genetic Testing|September 25, 1999
Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric communityK K Milner, T Han, E M Petty
Genetic Testing|September 25, 1999
A 6-year experience demonstrates the utility of screening for both cytogenetic and FMR-1 abnormalities in patients with mental retardationB J White, M Ayad, A Fraser, et al.
Genetic Testing|September 25, 1999
Prenatal diagnosis and the subsequent mutation analysis in a family with carbohydrate-deficient glycoprotein type I syndrome: growing evidence to support founder effects within CDG1 populationsA Crosby, S Jeffery, T Homfray, et al.
Genetic Testing|September 25, 1999
Disease genes and chromosomes: disease maps of the human genome. Chromosome 15F Gilbert
Genetic Testing|January 6, 2001
Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndromeJ Tzountzouris, D Kennedy, M Skuterud, et al.
Genetic Testing|January 6, 2001
Rapid mutation screening of phenylketonuria by polymerase chain reaction-linked restriction enzyme assay and direct sequence of the phenylalanine hydroxylase gene: clinical application in northern Japan and northern ChinaH Sueoka, M Nagao, S Chiba
Pageof 68