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Clinical genetics

Showing results (161-170 of 9,195) with videos related to

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Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.
Clinical Genetics|July 1, 1988
Recombinational event between Norrie disease and DXS7 lociJ T Ngo, M A Spence, V Cortessis, et al.
Clinical Genetics|October 3, 2020
Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defectsPing Yang, Changjian Yin, Mei Li, et al.
Clinical Genetics|April 5, 2020
Epigenetic variations due to nutritional status in early-life and its later impact on aging and diseaseJuan C Gomez-Verjan, Oscar S Barrera-Vázquez, Lizbeth García-Velázquez, et al.
Clinical Genetics|June 11, 2021
Novel CDK10 variants with multicystic dysplastic kidney, left ventricular non-compaction, and a solitary median maxillary central incisorClaude Darcha, Fanny Laffargue, Lucile Boutaud, et al.
Clinical Genetics|January 1, 1985
Balanced reciprocal translocations: risk factors for aneuploid segregant viabilityJ R Davis, B B Rogers, R M Hagaman, et al.
Clinical Genetics|September 1, 1985
Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathyH J Lin, J I Rotter, W J Conte
Clinical Genetics|May 1, 1986
Whole-arm t(X;17) (Xp17q;Xq17p) and gonadal dysgenesis. A further exception to the critical region hypothesisH Rivera, M A Enríquez-Guerra, A Rolón, et al.
Clinical Genetics|June 1, 1986
Partial deletion of the short arm of chromosome 3J L Tolmie, P Batstone, I Ruthven, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
Pageof 920

Showing results (161-170 of 9,195) with videos related to

Sort By:
Pageof 920
Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.
Clinical Genetics|July 1, 1988
Recombinational event between Norrie disease and DXS7 lociJ T Ngo, M A Spence, V Cortessis, et al.
Clinical Genetics|October 3, 2020
Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defectsPing Yang, Changjian Yin, Mei Li, et al.
Clinical Genetics|April 5, 2020
Epigenetic variations due to nutritional status in early-life and its later impact on aging and diseaseJuan C Gomez-Verjan, Oscar S Barrera-Vázquez, Lizbeth García-Velázquez, et al.
Clinical Genetics|June 11, 2021
Novel CDK10 variants with multicystic dysplastic kidney, left ventricular non-compaction, and a solitary median maxillary central incisorClaude Darcha, Fanny Laffargue, Lucile Boutaud, et al.
Clinical Genetics|January 1, 1985
Balanced reciprocal translocations: risk factors for aneuploid segregant viabilityJ R Davis, B B Rogers, R M Hagaman, et al.
Clinical Genetics|September 1, 1985
Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathyH J Lin, J I Rotter, W J Conte
Clinical Genetics|May 1, 1986
Whole-arm t(X;17) (Xp17q;Xq17p) and gonadal dysgenesis. A further exception to the critical region hypothesisH Rivera, M A Enríquez-Guerra, A Rolón, et al.
Clinical Genetics|June 1, 1986
Partial deletion of the short arm of chromosome 3J L Tolmie, P Batstone, I Ruthven, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
Pageof 920