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Social Science & Medicine (1982)
|
April 24, 2017
Discredited legacy: Stigma and familial amyloid polyneuropathy in Northwestern Portugal
Álvaro Mendes, Liliana Sousa, Jorge Sequeiros, et al.
Journal of Community Genetics
|
June 20, 2015
Challenges for providing genetic counselling in Colombian genetic clinics: the viewpoint of the physicians providing genetic consultations
Clemencia Rodas-Pérez, Angus Clarke, John Powell, et al.
Sociology of Health & Illness
|
January 29, 2026
Non-Directiveness and Authenticity in the Predictive Genetic Clinic
Shane Doheny, Rebecca Dimond, Lisa Ballard, et al.
European Journal of Human Genetics : EJHG
|
May 28, 2024
Written communication of whole genome sequencing results in the NHS Genomic Medicine Service: a multi-centre service evaluation
Holly Ellard, Angus Clarke, Sarah Wynn, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2015
How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence
Álvaro Mendes, Milena Paneque, Liliana Sousa, et al.
Sociology of Health & Illness
|
August 5, 2005
Dysmorphology and the spectacle of the clinic
Katie Featherstone, Joanna Latimer, Paul Atkinson, et al.
European Journal of Medical Genetics
|
November 30, 2018
Developing a short-form of the Genetic Counselling Outcome Scale: The Genomics Outcome Scale
Peter E Grant, Maria Pampaka, Katherine Payne, et al.
Medicine, Health Care, and Philosophy
|
August 29, 2006
The causation of disease - the practical and ethical consequences of competing explanations
Ulla Räisänen, Marie-Jet Bekkers, Paula Boddington, et al.
Journal of Autism and Developmental Disorders
|
April 26, 2015
Psychological Well-Being of Mothers and Siblings in Families of Girls and Women with Rett Syndrome
Rina Cianfaglione, Richard P Hastings, David Felce, et al.
European Journal of Human Genetics : EJHG
|
January 24, 2013
Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK)
Stuart J Moat, Donald M Bradley, Rachel Salmon, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 111) with videos related to
Sort By:
Page
of 12
Social Science & Medicine (1982)
|
April 24, 2017
Discredited legacy: Stigma and familial amyloid polyneuropathy in Northwestern Portugal
Álvaro Mendes, Liliana Sousa, Jorge Sequeiros, et al.
Journal of Community Genetics
|
June 20, 2015
Challenges for providing genetic counselling in Colombian genetic clinics: the viewpoint of the physicians providing genetic consultations
Clemencia Rodas-Pérez, Angus Clarke, John Powell, et al.
Sociology of Health & Illness
|
January 29, 2026
Non-Directiveness and Authenticity in the Predictive Genetic Clinic
Shane Doheny, Rebecca Dimond, Lisa Ballard, et al.
European Journal of Human Genetics : EJHG
|
May 28, 2024
Written communication of whole genome sequencing results in the NHS Genomic Medicine Service: a multi-centre service evaluation
Holly Ellard, Angus Clarke, Sarah Wynn, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2015
How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence
Álvaro Mendes, Milena Paneque, Liliana Sousa, et al.
Sociology of Health & Illness
|
August 5, 2005
Dysmorphology and the spectacle of the clinic
Katie Featherstone, Joanna Latimer, Paul Atkinson, et al.
European Journal of Medical Genetics
|
November 30, 2018
Developing a short-form of the Genetic Counselling Outcome Scale: The Genomics Outcome Scale
Peter E Grant, Maria Pampaka, Katherine Payne, et al.
Medicine, Health Care, and Philosophy
|
August 29, 2006
The causation of disease - the practical and ethical consequences of competing explanations
Ulla Räisänen, Marie-Jet Bekkers, Paula Boddington, et al.
Journal of Autism and Developmental Disorders
|
April 26, 2015
Psychological Well-Being of Mothers and Siblings in Families of Girls and Women with Rett Syndrome
Rina Cianfaglione, Richard P Hastings, David Felce, et al.
European Journal of Human Genetics : EJHG
|
January 24, 2013
Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK)
Stuart J Moat, Donald M Bradley, Rachel Salmon, et al.
Page
of 12