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Clinical genetics

Showing results (511-520 of 7,173) with videos related to

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Clinical Genetics|April 10, 2019
Brugada syndrome with SCN5A mutations exhibits more pronounced electrophysiological defects and more severe prognosis: A meta-analysisChen Chen, Zhaochong Tan, Wengen Zhu, et al.
Clinical Genetics|April 13, 2019
Clinical implications of the oncometabolite succinate in SDHx-mutation carriersKarin Eijkelenkamp, Thamara E Osinga, Thera P Links, et al.
Clinical Genetics|October 1, 1986
The arylsulphatases of chorionic villi: potential problems in the first-trimester diagnosis of metachromatic leucodystrophy and Maroteaux-Lamy diseaseN Sanguinetti, J Marsh, M Jackson, et al.
Clinical Genetics|May 1, 1986
Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysisM Schwartz, E Christensen, N C Christensen, et al.
Clinical Genetics|June 1, 1986
DNA polymorphisms around the apo AI gene in normal and hyperlipidaemic individuals selected for a twin studyA M Kessling, K Berg, E Mockleby, et al.
Clinical Genetics|June 1, 1977
X-linked aqueductal stenosisO Sovik, B van der Hagen, A C Loken
Clinical Genetics|August 29, 2018
A multicenter study to evaluate pulmonary function in osteogenesis imperfectaAllison Tam, Shan Chen, Evan Schauer, et al.
Clinical Genetics|September 15, 2018
Genetic screening for macular dystrophies in patients clinically diagnosed with dry age-related macular degenerationEveline Kersten, Maartje J Geerlings, Marc Pauper, et al.
Clinical Genetics|August 1, 1977
Alpha-I-antitrypsin (Pi) phenotypes in Lyon, France: departure from Hardy-Weinberg equilibriumP Arnaud, J P Pandey, H H Fudenberg, et al.
Clinical Genetics|June 22, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differencesE Brischoux-Boucher, A Trimouille, G Baujat, et al.
Pageof 718

Showing results (511-520 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|April 10, 2019
Brugada syndrome with SCN5A mutations exhibits more pronounced electrophysiological defects and more severe prognosis: A meta-analysisChen Chen, Zhaochong Tan, Wengen Zhu, et al.
Clinical Genetics|April 13, 2019
Clinical implications of the oncometabolite succinate in SDHx-mutation carriersKarin Eijkelenkamp, Thamara E Osinga, Thera P Links, et al.
Clinical Genetics|October 1, 1986
The arylsulphatases of chorionic villi: potential problems in the first-trimester diagnosis of metachromatic leucodystrophy and Maroteaux-Lamy diseaseN Sanguinetti, J Marsh, M Jackson, et al.
Clinical Genetics|May 1, 1986
Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysisM Schwartz, E Christensen, N C Christensen, et al.
Clinical Genetics|June 1, 1986
DNA polymorphisms around the apo AI gene in normal and hyperlipidaemic individuals selected for a twin studyA M Kessling, K Berg, E Mockleby, et al.
Clinical Genetics|June 1, 1977
X-linked aqueductal stenosisO Sovik, B van der Hagen, A C Loken
Clinical Genetics|August 29, 2018
A multicenter study to evaluate pulmonary function in osteogenesis imperfectaAllison Tam, Shan Chen, Evan Schauer, et al.
Clinical Genetics|September 15, 2018
Genetic screening for macular dystrophies in patients clinically diagnosed with dry age-related macular degenerationEveline Kersten, Maartje J Geerlings, Marc Pauper, et al.
Clinical Genetics|August 1, 1977
Alpha-I-antitrypsin (Pi) phenotypes in Lyon, France: departure from Hardy-Weinberg equilibriumP Arnaud, J P Pandey, H H Fudenberg, et al.
Clinical Genetics|June 22, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differencesE Brischoux-Boucher, A Trimouille, G Baujat, et al.
Pageof 718