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Angus J Clarke

Showing results (31-40 of 41) with videos related to

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Oncotarget|November 5, 2017
Somatic mutations in salivary duct carcinoma and potential therapeutic targetsTimothy K Khoo, Bing Yu, Joel A Smith, et al.
European Journal of Human Genetics : EJHG|April 24, 2018
Recontacting or not recontacting? A survey of current practices in clinical genetics centres in EuropeFabio Sirchia, Daniele Carrieri, Sandi Dheensa, et al.
Frontiers in Neurology|July 7, 2022
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency DisorderSam Amin, Marie Monaghan, Angel Aledo-Serrano, et al.
American Journal of Medical Genetics. Part A|February 1, 2019
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathwayJohn Timothy Wright, Mary Fete, Holm Schneider, et al.
European Journal of Human Genetics : EJHG|July 15, 2005
Early onset seizures and Rett-like features associated with mutations in CDKL5Julie C Evans, Hayley L Archer, James P Colley, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 3, 2017
Predictive testing of minors for Huntington's disease: The UK and Netherlands experiencesOliver W Quarrell, Angus J Clarke, Cecilia Compton, et al.
European Journal of Human Genetics : EJHG|October 13, 2018
Recontacting patients in clinical genetics services: recommendations of the European Society of Human GeneticsDaniele Carrieri, Heidi C Howard, Caroline Benjamin, et al.
European Journal of Human Genetics : EJHG|September 13, 2023
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new familiesVani Jain, Seow Hoong Foo, Stephen Chooi, et al.
European Journal of Human Genetics : EJHG|June 26, 2019
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac deathFlorence Fellmann, Carla G van El, Philippe Charron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Oncotarget|November 5, 2017
Somatic mutations in salivary duct carcinoma and potential therapeutic targetsTimothy K Khoo, Bing Yu, Joel A Smith, et al.
European Journal of Human Genetics : EJHG|April 24, 2018
Recontacting or not recontacting? A survey of current practices in clinical genetics centres in EuropeFabio Sirchia, Daniele Carrieri, Sandi Dheensa, et al.
Frontiers in Neurology|July 7, 2022
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency DisorderSam Amin, Marie Monaghan, Angel Aledo-Serrano, et al.
American Journal of Medical Genetics. Part A|February 1, 2019
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathwayJohn Timothy Wright, Mary Fete, Holm Schneider, et al.
European Journal of Human Genetics : EJHG|July 15, 2005
Early onset seizures and Rett-like features associated with mutations in CDKL5Julie C Evans, Hayley L Archer, James P Colley, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 3, 2017
Predictive testing of minors for Huntington's disease: The UK and Netherlands experiencesOliver W Quarrell, Angus J Clarke, Cecilia Compton, et al.
European Journal of Human Genetics : EJHG|October 13, 2018
Recontacting patients in clinical genetics services: recommendations of the European Society of Human GeneticsDaniele Carrieri, Heidi C Howard, Caroline Benjamin, et al.
European Journal of Human Genetics : EJHG|September 13, 2023
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new familiesVani Jain, Seow Hoong Foo, Stephen Chooi, et al.
European Journal of Human Genetics : EJHG|June 26, 2019
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac deathFlorence Fellmann, Carla G van El, Philippe Charron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Pageof 5