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Clinical genetics

Showing results (271-280 of 7,173) with videos related to

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Clinical Genetics|June 1, 1988
The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986H Veenema, G C Beverstock, T de Koning, et al.
Clinical Genetics|June 1, 1988
Heterogeneity of dominant high-frequency sensorineural deafnessK Higashi
Clinical Genetics|June 1, 1988
Unusual segregation in a family with a 11/21 translocationP Steensen, J H Ford, K Lillquist, et al.
Clinical Genetics|November 10, 2019
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutationFabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, et al.
Clinical Genetics|September 1, 1988
Defective polymorphonuclear chemotaxis in patients with Turner's syndrome (45,X)M López-Osuna, E Vega-Avila, F Salamanca, et al.
Clinical Genetics|September 1, 1988
Risk effect of maternal age in Pallister i(12p) syndromeS L Wenger, M W Steele, W D Yu
Clinical Genetics|September 1, 1988
Acid alpha-neuraminidase deficiency: a nephropathic phenotype?K S Roth, J C Chan, N R Ghatak, et al.
Clinical Genetics|September 1, 1988
Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XYU Kristoffersson, J Lagergren, S Heim, et al.
Clinical Genetics|December 14, 2019
Widening the spectrum of genetic testing in familial hypercholesterolaemia: Will it translate into better patient and population outcomes?Michael M Page, Damon A Bell, Gerald F Watts
Clinical Genetics|December 14, 2019
Uptake of polygenic risk information among women at increased risk of breast cancerTatiane Yanes, Bettina Meiser, Rajneesh Kaur, et al.
Pageof 718

Showing results (271-280 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|June 1, 1988
The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986H Veenema, G C Beverstock, T de Koning, et al.
Clinical Genetics|June 1, 1988
Heterogeneity of dominant high-frequency sensorineural deafnessK Higashi
Clinical Genetics|June 1, 1988
Unusual segregation in a family with a 11/21 translocationP Steensen, J H Ford, K Lillquist, et al.
Clinical Genetics|November 10, 2019
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutationFabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, et al.
Clinical Genetics|September 1, 1988
Defective polymorphonuclear chemotaxis in patients with Turner's syndrome (45,X)M López-Osuna, E Vega-Avila, F Salamanca, et al.
Clinical Genetics|September 1, 1988
Risk effect of maternal age in Pallister i(12p) syndromeS L Wenger, M W Steele, W D Yu
Clinical Genetics|September 1, 1988
Acid alpha-neuraminidase deficiency: a nephropathic phenotype?K S Roth, J C Chan, N R Ghatak, et al.
Clinical Genetics|September 1, 1988
Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XYU Kristoffersson, J Lagergren, S Heim, et al.
Clinical Genetics|December 14, 2019
Widening the spectrum of genetic testing in familial hypercholesterolaemia: Will it translate into better patient and population outcomes?Michael M Page, Damon A Bell, Gerald F Watts
Clinical Genetics|December 14, 2019
Uptake of polygenic risk information among women at increased risk of breast cancerTatiane Yanes, Bettina Meiser, Rajneesh Kaur, et al.
Pageof 718