Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?-Reference-Cited by-同舟云学术

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Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?

Published:2019-08-05 Issue:5 Volume:28 Page:1029-1041
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:Jrnl of Gene Coun

Author:

Taylor Shelby¹²³,Rodrigues Miriam⁴⁵,Poke Gemma⁶,Wake Samantha¹²,McEwen Alison⁷

Affiliation:

1. The Department of Paediatrics The University of Melbourne Melbourne Australia

2. Murdoch Children’s Research Institute Melbourne Australia

3. Parkville Familial Cancer Centre and Genomic Medicine Peter MacCallum Cancer Centre and The Royal Melbourne Hospital Melbourne Australia

4. Neurology Auckland District Health Board Auckland New Zealand

5. Muscular Dystrophy Association of New Zealand Auckland New Zealand

6. Genetic Health Services Wellington New Zealand

7. University of Technology Sydney Sydney Australia

Publisher

Wiley

Subject

Genetics(clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgc4.1156

Reference58 articles.

1. The right not to know: an autonomy based approach

2. Consensus-based care recommendations for adults with myotonic dystrophy type 1

3. Pregnancy course and outcome in women with hereditary neuromuscular disorders: comparison of obstetric risks in 178 patients

4. Adaptation to living with a genetic condition or risk: a mini-review

5. A Survey of Genetic Counselors' Strategies for Addressing Ethical and Professional Challenges in Practice

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinician perspectives on policy approaches to genetic risk disclosure in families;Familial Cancer;2024-03-28

2. Family Communication about Diagnostic Genetic Testing for Younger-Onset Dementia;Journal of Personalized Medicine;2023-04-01

3. Individual experiences and issues in predictive genetic testing for untreatable hereditary neuromuscular diseases in Japan;European Journal of Medical Genetics;2023-01

4. Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataract;Neuromuscular Disorders;2022-10

5. Disclosing genetic information to family members without consent: Five Australian case studies;European Journal of Medical Genetics;2020-11

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