Are we all of one mind? Clinicians' and patients' opinions regarding the development of a service protocol for predictive testing for Huntington disease

Author:

Copley Tobin T.,Wiggins Sandi,Dufrasne Suzanne,Bloch Maurice,Adam Shelin,McKellin William,Hayden Michael R.,

Publisher

Wiley

Subject

Genetics(clinical)

Reference17 articles.

1. Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene

2. Presymptomatic Diagnosis of Delayed-Onset Disease With Linked DNA Markers

3. Committee on Assessing Genetic Risks (1994): Financing of genetic testing and screening services. In (eds): “Assessing Genetic Risks: Implications for Health and Social Policy.” Division of Health Sciences Policy, Institute of Medicine, Washington, DC: National Academy Press.

4. Predictive testing for Huntington disease: I. Description of a pilot project in British Columbia

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1. Complexities in Genetic Counseling and Testing of Huntington's Disease: A Perspective from India;Neurology India;2022

2. Genetic counseling and testing for Huntington's disease: A historical review;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-05-13

3. Experience over fifteen years with a protocol for predictive testing for Huntington disease;Molecular Genetics and Metabolism;2011-04

4. Consumer contribution to the delivery of genetic health services;American Journal of Medical Genetics Part A;2008-09-01

5. GENETICS OF DEMENTIA;CONTINUUM: Lifelong Learning in Neurology;2008-04

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