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Clinical genetics

Showing results (101-110 of 9,193) with videos related to

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Clinical Genetics|November 1, 1989
Impact, logistics and prospects of traditional prenatal diagnosisW Furhmann
Clinical Genetics|November 1, 1989
Automated cytogenetic analysis: accomplishments, present status and practical future possibilitiesC Lundsteen, J Philip
Clinical Genetics|November 10, 2017
Biallelic mutations in mitochondrial tryptophanyl-tRNA synthetase cause Levodopa-responsive infantile-onset ParkinsonismE A Burke, S J Frucht, K Thompson, et al.
Clinical Genetics|July 30, 2016
Mutation in JPH2 cause dilated cardiomyopathyM Sabater-Molina, M Navarro, E García-Molina Sáez, et al.
Clinical Genetics|August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paragangliomaA S Hoekstra, B van den Ende, X P Julià, et al.
Clinical Genetics|August 11, 2016
Frameshift variant FANCL*c.1096_1099dupATTA is not associated with high breast cancer riskK Pfeifer, P Schürmann, N Bogdanova, et al.
Clinical Genetics|May 1, 1981
Association of the X chromosomal region q11 leads to 22 and Klinefelter syndromeS R Patil, J A Bartley, J W Hanson
Clinical Genetics|September 1, 1981
Klinefelter syndrome and the Xq11-22 regionJ P Fryns
Clinical Genetics|February 10, 2025
Progressive Cone-Rod Synaptic Dysfunction in Dynamin-1 (DNM1) Related Developmental and Epileptic Encephalopathy: A Distinct Retinal Phenotype in HumanOliver R Marmoy, Eleanor Hay, Richard Bowman, et al.
Clinical Genetics|February 16, 2025
Intrahepatic Cholestasis of Pregnancy: A Single-Centre Whole-Exome Sequencing Study in a Maltese CohortDorianne Spiteri, Laura Grech, Charles Savona-Ventura, et al.
Pageof 920

Showing results (101-110 of 9,193) with videos related to

Sort By:
Pageof 920
Clinical Genetics|November 1, 1989
Impact, logistics and prospects of traditional prenatal diagnosisW Furhmann
Clinical Genetics|November 1, 1989
Automated cytogenetic analysis: accomplishments, present status and practical future possibilitiesC Lundsteen, J Philip
Clinical Genetics|November 10, 2017
Biallelic mutations in mitochondrial tryptophanyl-tRNA synthetase cause Levodopa-responsive infantile-onset ParkinsonismE A Burke, S J Frucht, K Thompson, et al.
Clinical Genetics|July 30, 2016
Mutation in JPH2 cause dilated cardiomyopathyM Sabater-Molina, M Navarro, E García-Molina Sáez, et al.
Clinical Genetics|August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paragangliomaA S Hoekstra, B van den Ende, X P Julià, et al.
Clinical Genetics|August 11, 2016
Frameshift variant FANCL*c.1096_1099dupATTA is not associated with high breast cancer riskK Pfeifer, P Schürmann, N Bogdanova, et al.
Clinical Genetics|May 1, 1981
Association of the X chromosomal region q11 leads to 22 and Klinefelter syndromeS R Patil, J A Bartley, J W Hanson
Clinical Genetics|September 1, 1981
Klinefelter syndrome and the Xq11-22 regionJ P Fryns
Clinical Genetics|February 10, 2025
Progressive Cone-Rod Synaptic Dysfunction in Dynamin-1 (DNM1) Related Developmental and Epileptic Encephalopathy: A Distinct Retinal Phenotype in HumanOliver R Marmoy, Eleanor Hay, Richard Bowman, et al.
Clinical Genetics|February 16, 2025
Intrahepatic Cholestasis of Pregnancy: A Single-Centre Whole-Exome Sequencing Study in a Maltese CohortDorianne Spiteri, Laura Grech, Charles Savona-Ventura, et al.
Pageof 920