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Angus J Clarke

Showing results (21-30 of 41) with videos related to

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European Journal of Human Genetics : EJHG|July 5, 2007
Process and outcome in communication of genetic information within families: a systematic reviewClara L Gaff, Angus J Clarke, Paul Atkinson, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Second International Conference on a classification of ectodermal dysplasias: development of a multiaxis modelCarlos F Salinas, Alan D Irvine, Peter H Itin, et al.
Plos One|December 11, 2013
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmentiRachel E Towers, Leonardo Murgiano, David S Millar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 22, 2023
The evolving role of medical geneticists in the era of gene therapy: An urgency to prepareJerry Vockley, Nicola Brunetti-Pierri, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 28, 2023
Response to Beretich and BeretichJerry Vockley, Nicola Brunetti-Pierri, Wendy K Chung, et al.
Human Genomics|December 19, 2012
'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health careAngus J Clarke, David N Cooper, Michael Krawczak, et al.
Annals of Neurology|December 15, 2010
Rett syndrome: revised diagnostic criteria and nomenclatureJeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, et al.
Genes|December 23, 2022
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly UpdateNicolai Peschel, John T Wright, Maranke I Koster, et al.
European Journal of Medical Genetics|June 13, 2020
Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutationMartin A McClatchey, Zachary D du Toit, Rhys Vaughan, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|July 5, 2007
Process and outcome in communication of genetic information within families: a systematic reviewClara L Gaff, Angus J Clarke, Paul Atkinson, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Second International Conference on a classification of ectodermal dysplasias: development of a multiaxis modelCarlos F Salinas, Alan D Irvine, Peter H Itin, et al.
Plos One|December 11, 2013
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmentiRachel E Towers, Leonardo Murgiano, David S Millar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 22, 2023
The evolving role of medical geneticists in the era of gene therapy: An urgency to prepareJerry Vockley, Nicola Brunetti-Pierri, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 28, 2023
Response to Beretich and BeretichJerry Vockley, Nicola Brunetti-Pierri, Wendy K Chung, et al.
Human Genomics|December 19, 2012
'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health careAngus J Clarke, David N Cooper, Michael Krawczak, et al.
Annals of Neurology|December 15, 2010
Rett syndrome: revised diagnostic criteria and nomenclatureJeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, et al.
Genes|December 23, 2022
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly UpdateNicolai Peschel, John T Wright, Maranke I Koster, et al.
European Journal of Medical Genetics|June 13, 2020
Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutationMartin A McClatchey, Zachary D du Toit, Rhys Vaughan, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.
Pageof 5