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Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial

INTRODUCTION: Genetic testing for hypertrophic cardiomyopathy (HCM) in the era of genomics brings unique challenges for genetic counselling. The number of genes routinely included in an HCM gene panel has increased markedly, many with minimal if any robust evidence of gene–disease association. Subse...

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Publicat a:BMJ Open
Autors principals: Burns, Charlotte, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie
Format: Artigo
Idioma:Inglês
Publicat: BMJ Publishing Group 2019
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6361342/
https://ncbi.nlm.nih.gov/pubmed/30782759
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2018-026627
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