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Clinical genetics

Showing results (461-470 of 7,173) with videos related to

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Clinical Genetics|July 5, 2021
Hypermobile Ehlers-Danlos syndrome: A review and a critical appraisal of published genetic research to dateKirsty Scicluna, Melissa M Formosa, Rosienne Farrugia, et al.
Clinical Genetics|May 9, 2022
Carrier frequency of autosomal recessive genetic conditions in diverse populations: Lessons learned from the genome aggregation databaseMatthew J Schmitz, Mahmoud Aarabi, Ali Bashar, et al.
Clinical Genetics|July 23, 2021
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype-phenotype spectrum and functional impact on GPI-anchored proteinsSmrithi Salian, Marcello Scala, Thi Tuyet Mai Nguyen, et al.
Clinical Genetics|July 14, 2021
Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genesAlexandre Xavier, Rodney J Scott, Bente Talseth-Palmer
Clinical Genetics|March 1, 1988
X-linked lymphoproliferative disease: linkage studies using DNA probesA Harris, G M Lenoir, S A Lankester
Clinical Genetics|October 1, 1986
Inbreeding and schizophreniaL Saugstad, O Odegård
Clinical Genetics|October 1, 1986
An asymmetric type of chondrodysplasia in an adult male. Another example of postzygotic mutation for an autosomal dominant gene?J P Fryns, H van den Berghe
Clinical Genetics|November 1, 1986
Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testesE Lieber, S S Wachtel, B Aftalion, et al.
Clinical Genetics|December 1, 1986
Ehlers-Danlos features with progeroid facies and mild mental retardation. Further delineation of the syndromeA Hernández, M G Aguirre-Negrete, S González-Flores, et al.
Clinical Genetics|December 1, 1986
Ring 21 chromosome: the mild end of the phenotypic spectrumR J Gardner, N A Monk, J E Clarkson, et al.
Pageof 718

Showing results (461-470 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|July 5, 2021
Hypermobile Ehlers-Danlos syndrome: A review and a critical appraisal of published genetic research to dateKirsty Scicluna, Melissa M Formosa, Rosienne Farrugia, et al.
Clinical Genetics|May 9, 2022
Carrier frequency of autosomal recessive genetic conditions in diverse populations: Lessons learned from the genome aggregation databaseMatthew J Schmitz, Mahmoud Aarabi, Ali Bashar, et al.
Clinical Genetics|July 23, 2021
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype-phenotype spectrum and functional impact on GPI-anchored proteinsSmrithi Salian, Marcello Scala, Thi Tuyet Mai Nguyen, et al.
Clinical Genetics|July 14, 2021
Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genesAlexandre Xavier, Rodney J Scott, Bente Talseth-Palmer
Clinical Genetics|March 1, 1988
X-linked lymphoproliferative disease: linkage studies using DNA probesA Harris, G M Lenoir, S A Lankester
Clinical Genetics|October 1, 1986
Inbreeding and schizophreniaL Saugstad, O Odegård
Clinical Genetics|October 1, 1986
An asymmetric type of chondrodysplasia in an adult male. Another example of postzygotic mutation for an autosomal dominant gene?J P Fryns, H van den Berghe
Clinical Genetics|November 1, 1986
Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testesE Lieber, S S Wachtel, B Aftalion, et al.
Clinical Genetics|December 1, 1986
Ehlers-Danlos features with progeroid facies and mild mental retardation. Further delineation of the syndromeA Hernández, M G Aguirre-Negrete, S González-Flores, et al.
Clinical Genetics|December 1, 1986
Ring 21 chromosome: the mild end of the phenotypic spectrumR J Gardner, N A Monk, J E Clarkson, et al.
Pageof 718