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Felicity K Boardman

Showing results (1-10 of 22) with videos related to

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Journal of Genetic Counseling|November 13, 2020
Attitudes toward population screening among people living with fragile X syndrome in the UK: 'I wouldn't wish him away, I'd just wish his fragile X syndrome away'Felicity K Boardman
Social Science & Medicine (1982)|September 20, 2017
Experience as knowledge: Disability, distillation and (reprogenetic) decision-makingFelicity K Boardman
Acta Paediatrica (Oslo, Norway : 1992)|May 3, 2020
Whose life is worth preserving? Disabled people and the expressivist objection to neonatologyFelicity K Boardman
Sociology of Health & Illness|October 12, 2013
Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisionsFelicity K Boardman
Social Science & Medicine (1982)|November 16, 2010
Accessing the field: Disability and the research processLindsey Brown, Felicity K Boardman
Molecular Genetics & Genomic Medicine|September 10, 2018
How do genetically disabled adults view selective reproduction? Impairment, identity, and genetic screeningFelicity K Boardman, Rachel Hale
Journal of Genetic Counseling|January 11, 2019
"I didn't take it too seriously because I'd just never heard of it": Experiential knowledge and genetic screening for thalassaemia in the UKFelicity K Boardman, Rachel Hale
European Journal of Human Genetics : EJHG|September 27, 2021
What is a 'serious' genetic condition? The perceptions of people living with genetic conditionsFelicity K Boardman, Corinna C Clark
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 1, 2019
Newborn screening for haemophilia: The views of families and adults living with haemophilia in the UKFelicity K Boardman, Rachel Hale, Philip J Young
Molecular Genetics & Genomic Medicine|November 24, 2017
Newborn genetic screening for spinal muscular atrophy in the UK: The views of the general populationFelicity K Boardman, Chloe Sadler, Philip J Young
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Genetic Counseling|November 13, 2020
Attitudes toward population screening among people living with fragile X syndrome in the UK: 'I wouldn't wish him away, I'd just wish his fragile X syndrome away'Felicity K Boardman
Social Science & Medicine (1982)|September 20, 2017
Experience as knowledge: Disability, distillation and (reprogenetic) decision-makingFelicity K Boardman
Acta Paediatrica (Oslo, Norway : 1992)|May 3, 2020
Whose life is worth preserving? Disabled people and the expressivist objection to neonatologyFelicity K Boardman
Sociology of Health & Illness|October 12, 2013
Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisionsFelicity K Boardman
Social Science & Medicine (1982)|November 16, 2010
Accessing the field: Disability and the research processLindsey Brown, Felicity K Boardman
Molecular Genetics & Genomic Medicine|September 10, 2018
How do genetically disabled adults view selective reproduction? Impairment, identity, and genetic screeningFelicity K Boardman, Rachel Hale
Journal of Genetic Counseling|January 11, 2019
"I didn't take it too seriously because I'd just never heard of it": Experiential knowledge and genetic screening for thalassaemia in the UKFelicity K Boardman, Rachel Hale
European Journal of Human Genetics : EJHG|September 27, 2021
What is a 'serious' genetic condition? The perceptions of people living with genetic conditionsFelicity K Boardman, Corinna C Clark
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 1, 2019
Newborn screening for haemophilia: The views of families and adults living with haemophilia in the UKFelicity K Boardman, Rachel Hale, Philip J Young
Molecular Genetics & Genomic Medicine|November 24, 2017
Newborn genetic screening for spinal muscular atrophy in the UK: The views of the general populationFelicity K Boardman, Chloe Sadler, Philip J Young
Pageof 3