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Clinical genetics

Showing results (221-230 of 7,173) with videos related to

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Clinical Genetics|May 10, 2002
Two novel mutations in the sterol 27-hydroxylase gene causing cerebrotendinous xanthomatosisS Lamon-Fava, E J Schaefer, R Garuti, et al.
Clinical Genetics|May 20, 2003
Vascular malformations: localized defects in vascular morphogenesisP Brouillard, M Vikkula
Clinical Genetics|May 20, 2003
Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked traitM Tadin-Strapps, J C Salas-Alanis, L Moreno, et al.
Clinical Genetics|April 16, 2003
The allelic loss of chromosome 3p25 with c-myc gain is related to the development of clear-cell renal cell carcinomaS Yamaguchi, S Yoshihiro, H Matsuyama, et al.
Clinical Genetics|April 16, 2003
Two novel mutations in the alpha-galactosidase A gene in Chinese patients with Fabry diseaseC-C Yang, L-W Lai, O Whitehair, et al.
Clinical Genetics|April 16, 2003
Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2R E Pyatt, H Nakagawa, H Hampel, et al.
Clinical Genetics|June 7, 2003
Association of the myocilin mt.1 promoter variant with the worsening of glaucomatous disease over timeJ R Polansky, R P Juster, G L Spaeth
Clinical Genetics|June 7, 2003
Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the VikingsN Milman, P Pedersen
Clinical Genetics|June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000S Creighton, E W Almqvist, D MacGregor, et al.
Clinical Genetics|June 6, 2003
Analysis of splice-site mutations of the alpha-galactosidase A gene in Fabry diseaseL-W Lai, O Whitehair, M-J Wu, et al.
Pageof 718

Showing results (221-230 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|May 10, 2002
Two novel mutations in the sterol 27-hydroxylase gene causing cerebrotendinous xanthomatosisS Lamon-Fava, E J Schaefer, R Garuti, et al.
Clinical Genetics|May 20, 2003
Vascular malformations: localized defects in vascular morphogenesisP Brouillard, M Vikkula
Clinical Genetics|May 20, 2003
Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked traitM Tadin-Strapps, J C Salas-Alanis, L Moreno, et al.
Clinical Genetics|April 16, 2003
The allelic loss of chromosome 3p25 with c-myc gain is related to the development of clear-cell renal cell carcinomaS Yamaguchi, S Yoshihiro, H Matsuyama, et al.
Clinical Genetics|April 16, 2003
Two novel mutations in the alpha-galactosidase A gene in Chinese patients with Fabry diseaseC-C Yang, L-W Lai, O Whitehair, et al.
Clinical Genetics|April 16, 2003
Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2R E Pyatt, H Nakagawa, H Hampel, et al.
Clinical Genetics|June 7, 2003
Association of the myocilin mt.1 promoter variant with the worsening of glaucomatous disease over timeJ R Polansky, R P Juster, G L Spaeth
Clinical Genetics|June 7, 2003
Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the VikingsN Milman, P Pedersen
Clinical Genetics|June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000S Creighton, E W Almqvist, D MacGregor, et al.
Clinical Genetics|June 6, 2003
Analysis of splice-site mutations of the alpha-galactosidase A gene in Fabry diseaseL-W Lai, O Whitehair, M-J Wu, et al.
Pageof 718