Birth after pre-implantation genetic diagnosis (PGD) of spinocerebellar ataxia 2 (Sca2)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference15 articles.
1. Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)n repeat detection
2. Diseases of Unstable Repeat Expansion: Mechanisms and Common Principles
3. THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS
4. Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis
5. New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications
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1. PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical cases;Journal of Assisted Reproduction and Genetics;2024-04-05
2. A comprehensive review of iPS cell line-based disease modelling of the polyglutamine spinocerebellar ataxias 2 and 3: a focus on the research outcomes;Annals of Medicine & Surgery;2024-03-19
3. Review: Preimplantation genetic diagnosis (PGD) as a reproductive option in patients with neurodegenerative disorders;Reproductive Biology;2021-03
4. Live births following preimplantation genetic testing for dynamic mutation diseases by karyomapping: a report of three cases;Journal of Assisted Reproduction and Genetics;2020-03
5. Movement disorders in pregnancy;Handbook of Clinical Neurology;2020
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