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Lyn S Chitty

Showing results (201-210 of 225) with videos related to

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Orphanet Journal of Rare Diseases|September 9, 2024
Preferences for coordinated care for rare diseases: discrete choice experimentStephen Morris, Holly Walton, Amy Simpson, et al.
Orphanet Journal of Rare Diseases|November 24, 2023
Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionalsHolly Walton, Pei Li Ng, Amy Simpson, et al.
BMC Pregnancy and Childbirth|February 11, 2026
"You think everything's fine and then it starts not being fine": a qualitative descriptive study exploring the prenatal testing experiences of Black women living in EnglandMichelle Peter, Clotilde Abe, Agnes Agyepong, et al.
Prenatal Diagnosis|April 27, 2022
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice surveyJames Buchanan, Melissa Hill, Caroline M Vass, et al.
Lancet (London, England)|August 12, 2009
Post-mortem examination of human fetuses: a comparison of whole-body high-field MRI at 9.4 T with conventional MRI and invasive autopsySudhin Thayyil, Jon O Cleary, Neil J Sebire, et al.
European Journal of Human Genetics : EJHG|November 4, 2024
"I'm quite proud of how we've handled it": health professionals' experiences of returning additional findings from the 100,000 genomes projectBethany Stafford-Smith, Jana Gurasashvili, Michelle Peter, et al.
European Radiology|October 23, 2015
Comparison of diagnostic performance for perinatal and paediatric post-mortem imaging: CT versus MRIOwen J Arthurs, Anna Guy, Sudhin Thayyil, et al.
Lancet (London, England)|May 21, 2013
Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation studySudhin Thayyil, Neil J Sebire, Lyn S Chitty, et al.
Health and Social Care Delivery Research|April 29, 2026
Optimising rapid prenatal exome sequencing in the NHS genomic medicine service: the EXPRESS SynopsisMelissa Hill, Michelle Peter, Morgan Daniel, 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.
Pageof 23

Showing results (201-210 of 225) with videos related to

Sort By:
Pageof 23
Orphanet Journal of Rare Diseases|September 9, 2024
Preferences for coordinated care for rare diseases: discrete choice experimentStephen Morris, Holly Walton, Amy Simpson, et al.
Orphanet Journal of Rare Diseases|November 24, 2023
Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionalsHolly Walton, Pei Li Ng, Amy Simpson, et al.
BMC Pregnancy and Childbirth|February 11, 2026
"You think everything's fine and then it starts not being fine": a qualitative descriptive study exploring the prenatal testing experiences of Black women living in EnglandMichelle Peter, Clotilde Abe, Agnes Agyepong, et al.
Prenatal Diagnosis|April 27, 2022
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice surveyJames Buchanan, Melissa Hill, Caroline M Vass, et al.
Lancet (London, England)|August 12, 2009
Post-mortem examination of human fetuses: a comparison of whole-body high-field MRI at 9.4 T with conventional MRI and invasive autopsySudhin Thayyil, Jon O Cleary, Neil J Sebire, et al.
European Journal of Human Genetics : EJHG|November 4, 2024
"I'm quite proud of how we've handled it": health professionals' experiences of returning additional findings from the 100,000 genomes projectBethany Stafford-Smith, Jana Gurasashvili, Michelle Peter, et al.
European Radiology|October 23, 2015
Comparison of diagnostic performance for perinatal and paediatric post-mortem imaging: CT versus MRIOwen J Arthurs, Anna Guy, Sudhin Thayyil, et al.
Lancet (London, England)|May 21, 2013
Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation studySudhin Thayyil, Neil J Sebire, Lyn S Chitty, et al.
Health and Social Care Delivery Research|April 29, 2026
Optimising rapid prenatal exome sequencing in the NHS genomic medicine service: the EXPRESS SynopsisMelissa Hill, Michelle Peter, Morgan Daniel, 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.
Pageof 23