Personal utility of genomic sequencing for infants with congenital deafness-Reference-Cited by-同舟云学术

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Personal utility of genomic sequencing for infants with congenital deafness

Published:2021-06-29 Issue:12 Volume:185 Page:3634-3643
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Tutty Erin¹²,Amor David J.¹²³⁴,Jarmolowicz Anna²⁵^ORCID,Paton Kate²,Downie Lilian¹²^ORCID

Affiliation:

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

2. Murdoch Children's Research Institute Melbourne Victoria Australia

3. Royal Children's Hospital Parkville Victoria Australia

4. Victorian Clinical Genetics Service Melbourne Victoria Australia

5. Melbourne Genomics Health Alliance Melbourne Victoria Australia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62411

Reference30 articles.

1. What do patients with hereditary deafness think of genetic studies?

2. Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?

3. The Implications of Genetic Testing for Deafness

4. Deaf Adults' Reasons for Genetic Testing Depend on Cultural Affiliation: Results From a Prospective, Longitudinal Genetic Counseling and Testing Study

5. Genetic Testing and Genetic Counseling for Deafness: The Future Is Here

Cited by 7 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. Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population;Human Genetics and Genomics Advances;2024-07

2. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care;The Journal of Pediatrics;2023-10

3. An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech;Journal of Speech, Language, and Hearing Research;2023-09-15

4. Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss;The Laryngoscope;2022-12-14

5. From newborn screening to genomic medicine: challenges and suggestions on how to incorporate genomic newborn screening in public health programs;Medizinische Genetik;2022-04-01

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