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European Journal of Human Genetics : EJHG
|
June 15, 2007
An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countries
Celine Lewis, Pritti Mehta, Alastair Kent, et al.
European Journal of Human Genetics : EJHG
|
November 21, 2013
What hinders minority ethnic access to cancer genetics services and what may help?
Anna Allford, Nadeem Qureshi, Julian Barwell, et al.
American Journal of Medical Genetics. Part A
|
May 23, 2013
Views and preferences for the implementation of non-invasive prenatal diagnosis for single gene disorders from health professionals in the United Kingdom
Melissa Hill, Madhavi Karunaratna, Celine Lewis, et al.
Journal of Health Psychology
|
January 29, 2024
'Don't let it hold you back' - The experience of transition to adulthood in young people with primary ciliary dyskinesia: An interpretative phenomenological analysis
Rhys Dore, Isabella E Nizza, Hannah M Mitchison, et al.
Prenatal Diagnosis
|
May 4, 2020
Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, et al.
Journal of Genetic Counseling
|
August 6, 2025
Anxiety and quality-of-life for parents of children with undiagnosed rare conditions: A multi-site quantitative survey study
Ria Patel, Bettina Friedrich, Saskia C Sanderson, et al.
BMC Pregnancy and Childbirth
|
April 29, 2017
Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study
Kerry Oxenford, Rebecca Daley, Celine Lewis, et al.
Journal of Medical Genetics
|
February 12, 2025
Parental knowledge, attitudes, satisfaction and decisional conflict regarding whole genome sequencing in the Genomic Medicine Service: a multisite survey study in England
Ria Patel, Bettina Friedrich, Saskia C Sanderson, et al.
Journal of Medical Genetics
|
December 11, 2025
Challenges associated with disclosing results from whole genome sequencing to diagnose paediatric rare diseases: analysis of parent-clinician interactions
Holly Ellard, Jhumana Ali, Phoebe Buxton, et al.
Prenatal Diagnosis
|
August 13, 2015
Non-invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers
Heather Skirton, Lesley Goldsmith, Leigh Jackson, et al.
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of 9
Search research articles
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Showing results (31-40 of 88) with videos related to
Sort By:
Page
of 9
European Journal of Human Genetics : EJHG
|
June 15, 2007
An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countries
Celine Lewis, Pritti Mehta, Alastair Kent, et al.
European Journal of Human Genetics : EJHG
|
November 21, 2013
What hinders minority ethnic access to cancer genetics services and what may help?
Anna Allford, Nadeem Qureshi, Julian Barwell, et al.
American Journal of Medical Genetics. Part A
|
May 23, 2013
Views and preferences for the implementation of non-invasive prenatal diagnosis for single gene disorders from health professionals in the United Kingdom
Melissa Hill, Madhavi Karunaratna, Celine Lewis, et al.
Journal of Health Psychology
|
January 29, 2024
'Don't let it hold you back' - The experience of transition to adulthood in young people with primary ciliary dyskinesia: An interpretative phenomenological analysis
Rhys Dore, Isabella E Nizza, Hannah M Mitchison, et al.
Prenatal Diagnosis
|
May 4, 2020
Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, et al.
Journal of Genetic Counseling
|
August 6, 2025
Anxiety and quality-of-life for parents of children with undiagnosed rare conditions: A multi-site quantitative survey study
Ria Patel, Bettina Friedrich, Saskia C Sanderson, et al.
BMC Pregnancy and Childbirth
|
April 29, 2017
Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study
Kerry Oxenford, Rebecca Daley, Celine Lewis, et al.
Journal of Medical Genetics
|
February 12, 2025
Parental knowledge, attitudes, satisfaction and decisional conflict regarding whole genome sequencing in the Genomic Medicine Service: a multisite survey study in England
Ria Patel, Bettina Friedrich, Saskia C Sanderson, et al.
Journal of Medical Genetics
|
December 11, 2025
Challenges associated with disclosing results from whole genome sequencing to diagnose paediatric rare diseases: analysis of parent-clinician interactions
Holly Ellard, Jhumana Ali, Phoebe Buxton, et al.
Prenatal Diagnosis
|
August 13, 2015
Non-invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers
Heather Skirton, Lesley Goldsmith, Leigh Jackson, et al.
Page
of 9