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Clinical genetics

Showing results (631-640 of 7,173) with videos related to

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Clinical Genetics|April 27, 2000
A germline mutation at the extreme 3' end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumorJ Couture, A Mitri, R Lagace, et al.
Clinical Genetics|April 27, 2000
Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemiaJ A Shin, S H Kim, U K Kim, et al.
Clinical Genetics|April 12, 2001
Sex determination: lessons from families and embryosH Ostrer
Clinical Genetics|April 12, 2001
Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathyJ Zhang, A Kumar, H J Stalker, et al.
Clinical Genetics|April 12, 2001
Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18pE M McGhee, Y Qu, M M Wohlferd, et al.
Clinical Genetics|May 22, 2001
The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndromeZ R Yuan, M Okaniwa, I Nagata, et al.
Clinical Genetics|May 22, 2001
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophyJ Finsterer, E Gharehbaghi-Schnell, C Stöllberger, et al.
Clinical Genetics|January 10, 2001
Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levelsO Aras, N Q Hanson, F Yang, et al.
Clinical Genetics|January 10, 2001
Segregation of a supernumerary del(15) marker chromosome in spermP D Cotter, E Ko, S K Larabell, et al.
Clinical Genetics|February 1, 1975
Isochromosome for the short arm of X: a human mosaic 45,x/46,XXpiP H Fitzgerald, R A Donald
Pageof 718

Showing results (631-640 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|April 27, 2000
A germline mutation at the extreme 3' end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumorJ Couture, A Mitri, R Lagace, et al.
Clinical Genetics|April 27, 2000
Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemiaJ A Shin, S H Kim, U K Kim, et al.
Clinical Genetics|April 12, 2001
Sex determination: lessons from families and embryosH Ostrer
Clinical Genetics|April 12, 2001
Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathyJ Zhang, A Kumar, H J Stalker, et al.
Clinical Genetics|April 12, 2001
Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18pE M McGhee, Y Qu, M M Wohlferd, et al.
Clinical Genetics|May 22, 2001
The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndromeZ R Yuan, M Okaniwa, I Nagata, et al.
Clinical Genetics|May 22, 2001
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophyJ Finsterer, E Gharehbaghi-Schnell, C Stöllberger, et al.
Clinical Genetics|January 10, 2001
Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levelsO Aras, N Q Hanson, F Yang, et al.
Clinical Genetics|January 10, 2001
Segregation of a supernumerary del(15) marker chromosome in spermP D Cotter, E Ko, S K Larabell, et al.
Clinical Genetics|February 1, 1975
Isochromosome for the short arm of X: a human mosaic 45,x/46,XXpiP H Fitzgerald, R A Donald
Pageof 718