Heterozygote screening for Tay-Sachs disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Cited by 22 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. The Evolving Landscape of Genetic Carrier Screening: Clinical Considerations and Challenges;Obstetrical & Gynecological Survey;2023-08
2. Patients' reactions and follow-up testing decisions related to Tay-Sachs (HEXA ) variants of uncertain significance results;Journal of Genetic Counseling;2019-03-07
3. Ashkenazi Jewish population screening for Tay-Sachs disease: The International and Australian experience;Journal of Paediatrics and Child Health;2014-06-13
4. Next‐generation DNA sequencing of HEXA : a step in the right direction for carrier screening;Molecular Genetics & Genomic Medicine;2013-09-16
5. The Gangliosidoses;Lysosomal Storage Disorders;2012-11-15
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