Exploring the complex attitudes of stakeholders to the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening

被引：0
|
作者：
Freeman, Lucinda [1 ,2 ]
Delatycki, Martin [3 ,4 ]
Scully, Jackie Leach [5 ]
Kirk, Edwin [2 ,6 ]
机构：
[1] Univ Technol Sydney, Grad Sch Hlth, Ultimo, Australia
[2] UNSW Sydney, Sch Womens & Childrens Hlth, Fac Med, Sydney, NSW, Australia
[3] Victorian Clin Genet Serv, Parkville, Vic, Australia
[4] Murdoch Childrens Res Inst, Parkville, Vic, Australia
[5] UNSW Sydney, Disabil Innovat Inst, Sydney, NSW, Australia
[6] Sydney Childrens Hosp, Clin Genet Ctr, Randwick, NSW, Australia
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P24.034.B
引用
收藏
页码：1840 / 1840
页数：1
相关论文
共 50 条
  • [1] Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
    Lucinda Freeman
    Martin B. Delatycki
    Jackie Leach Scully
    Nancy Briggs
    Edwin P. Kirk
    European Journal of Human Genetics, 2023, 31 : 548 - 554
  • [2] Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
    Freeman, Lucinda
    Delatycki, Martin B.
    Scully, Jackie Leach
    Briggs, Nancy
    Kirk, Edwin P.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 (05) : 548 - 554
  • [3] Views of reproductive genetic carrier screening participants regarding screening for genes associated with non-syndromic hearing loss
    Freeman, Lucinda
    Delatycki, Martin B.
    Scully, Jackie Leach
    Kirk, Edwin P.
    PRENATAL DIAGNOSIS, 2022, 42 (13) : 1658 - 1666
  • [4] Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness
    Freeman, Lucinda
    Bristowe, Lisa
    Kirk, Edwin P.
    Delatycki, Martin B.
    Scully, Jackie Leach
    JOURNAL OF GENETIC COUNSELING, 2024, 33 (03) : 566 - 577
  • [5] Genetic Non-Syndromic Hearing Loss in Turkey
    Bayazit, Yildirim A.
    JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY, 2011, 7 (03): : 357 - 360
  • [6] Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusis
    Cornejo-Sanchez, Diana M.
    Bharadwaj, Thashi
    Dong, Rui
    Wang, Gao T.
    Schrauwen, Isabelle
    Dewan, Andrew T.
    Leal, Suzanne M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2025,
  • [7] Genetic etiology of non-syndromic hearing loss in Europe
    del Castillo, Ignacio
    Morin, Matias
    Dominguez-Ruiz, Maria
    Moreno-Pelayo, Miguel A.
    HUMAN GENETICS, 2022, 141 (3-4) : 683 - 696
  • [8] Genetic and clinical diagnosis in non-syndromic hearing loss
    Sommen, Manou
    Van Camp, Guy
    Boudewyns, An
    HEARING BALANCE AND COMMUNICATION, 2013, 11 (03) : 138 - 145
  • [9] Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
    Doll, Julia
    Vona, Barbara
    Schnapp, Linda
    Rueschendorf, Franz
    Khan, Imran
    Khan, Saadullah
    Muhammad, Noor
    Alam Khan, Sher
    Nawaz, Hamed
    Khan, Ajmal
    Ahmad, Naseer
    Kolb, Susanne M.
    Kuehlewein, Laura
    Labonne, Jonathan D. J.
    Layman, Lawrence C.
    Hofrichter, Michaela A. H.
    Roder, Tabea
    Dittrich, Marcus
    Mueller, Tobias
    Graves, Tyler D.
    Kong, Il-Keun
    Nanda, Indrajit
    Kim, Hyung-Goo
    Haaf, Thomas
    GENES, 2020, 11 (11) : 1 - 16
  • [10] Genetic etiology of non-syndromic hearing loss in Europe
    Ignacio del Castillo
    Matías Morín
    María Domínguez-Ruiz
    Miguel A. Moreno-Pelayo
    Human Genetics, 2022, 141 : 683 - 696
12345