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Matthew E Hurles

Showing results (31-40 of 188) with videos related to

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Human Genetics|February 21, 2003
High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysisElena Bosch, Francesc Calafell, Zoë H Rosser, et al.
Nature Methods|May 25, 2006
Assaying chromosomal inversions by single-molecule haplotypingDaniel J Turner, Jay Shendure, Greg Porreca, et al.
HGG Advances|December 23, 2022
IMPROVE-DD: Integrating multiple phenotype resources optimizes variant evaluation in genetically determined developmental disordersStuart Aitken, Helen V Firth, Caroline F Wright, et al.
American Journal of Human Genetics|March 20, 2003
Native American Y chromosomes in Polynesia: the genetic impact of the Polynesian slave tradeMatthew E Hurles, Emma Maund, Jane Nicholson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2020
Evaluating variants classified as pathogenic in ClinVar in the DDD StudyCaroline F Wright, Ruth Y Eberhardt, Panayiotis Constantinou, et al.
Prenatal Diagnosis|August 24, 2016
Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representativesElizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, et al.
European Journal of Human Genetics : EJHG|April 30, 2015
Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing researchAnna Middleton, Katherine I Morley, Eugene Bragin, et al.
Journal of Medical Genetics|May 22, 2015
Potential research participants support the return of raw sequence dataAnna Middleton, Caroline F Wright, Katherine I Morley, et al.
Lancet (London, England)|December 23, 2014
No expectation to share incidental findings in genomic researchAnna Middleton, Katherine I Morley, Eugene Bragin, et al.
Nature Genetics|April 6, 2010
Mutation spectrum revealed by breakpoint sequencing of human germline CNVsDonald F Conrad, Christine Bird, Ben Blackburne, et al.
Pageof 19

Showing results (31-40 of 188) with videos related to

Sort By:
Pageof 19
Human Genetics|February 21, 2003
High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysisElena Bosch, Francesc Calafell, Zoë H Rosser, et al.
Nature Methods|May 25, 2006
Assaying chromosomal inversions by single-molecule haplotypingDaniel J Turner, Jay Shendure, Greg Porreca, et al.
HGG Advances|December 23, 2022
IMPROVE-DD: Integrating multiple phenotype resources optimizes variant evaluation in genetically determined developmental disordersStuart Aitken, Helen V Firth, Caroline F Wright, et al.
American Journal of Human Genetics|March 20, 2003
Native American Y chromosomes in Polynesia: the genetic impact of the Polynesian slave tradeMatthew E Hurles, Emma Maund, Jane Nicholson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2020
Evaluating variants classified as pathogenic in ClinVar in the DDD StudyCaroline F Wright, Ruth Y Eberhardt, Panayiotis Constantinou, et al.
Prenatal Diagnosis|August 24, 2016
Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representativesElizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, et al.
European Journal of Human Genetics : EJHG|April 30, 2015
Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing researchAnna Middleton, Katherine I Morley, Eugene Bragin, et al.
Journal of Medical Genetics|May 22, 2015
Potential research participants support the return of raw sequence dataAnna Middleton, Caroline F Wright, Katherine I Morley, et al.
Lancet (London, England)|December 23, 2014
No expectation to share incidental findings in genomic researchAnna Middleton, Katherine I Morley, Eugene Bragin, et al.
Nature Genetics|April 6, 2010
Mutation spectrum revealed by breakpoint sequencing of human germline CNVsDonald F Conrad, Christine Bird, Ben Blackburne, et al.
Pageof 19