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Heidi C Howard

Showing results (31-40 of 42) with videos related to

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European Journal of Human Genetics : EJHG|July 3, 2013
Whole-genome sequencing in health care. Recommendations of the European Society of Human GeneticsCarla G van El, Martina C Cornel, Pascal Borry, et al.
Personalized Medicine|June 2, 2018
'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methodsAnna Middleton, Emilia Niemiec, Barbara Prainsack, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.
European Journal of Human Genetics : EJHG|April 2, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendationsWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG|October 16, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, 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.
Nature Genetics|October 9, 2002
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosumHeidi C Howard, David B Mount, Daniel Rochefort, 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.
Genome Medicine|May 26, 2021
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countriesRichard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|July 3, 2013
Whole-genome sequencing in health care. Recommendations of the European Society of Human GeneticsCarla G van El, Martina C Cornel, Pascal Borry, et al.
Personalized Medicine|June 2, 2018
'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methodsAnna Middleton, Emilia Niemiec, Barbara Prainsack, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.
European Journal of Human Genetics : EJHG|April 2, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendationsWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG|October 16, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, 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.
Nature Genetics|October 9, 2002
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosumHeidi C Howard, David B Mount, Daniel Rochefort, 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.
Genome Medicine|May 26, 2021
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countriesRichard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Pageof 5