Molecular heterogeneity of the fragile X syndrome-Reference-Cited by-同舟云学术

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Molecular heterogeneity of the fragile X syndrome

Published:1991 Issue:16 Volume:19 Page:4355-4359
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucl Acids Res

Author:

Nakahori Y.,Knight S.J.L.,Holland J.,Schwartz C.,Roche A.,Tarleton J.,Wong S.,Flint T.J.,Froster-Iskenius U.,Bentley D.,Davies K.E.,Hirst M.C.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/19/16/4355/7075822/19-16-4355.pdf

Cited by 92 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. Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome;International Journal of Molecular Sciences;2023-05-24

2. Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG);Genetics in Medicine;2021-05

3. Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation;European Journal of Human Genetics;2019-12-05

4. Clinical Genetic Testing for Fragile X Syndrome by Polymerase Chain Reaction Amplification and Southern Blot Analyses;Fragile-X Syndrome;2019

5. Development of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion Mutations;Genes;2016-11-30

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