Fragile X syndrome: An overview and update of the FMR1 gene-Reference-Cited by-同舟云学术

Fragile X syndrome: An overview and update of the FMR1 gene

Published:2017-10-01 Issue:2 Volume:93 Page:197-205
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Mila M.¹²,Alvarez-Mora M.I.¹²,Madrigal I.¹²,Rodriguez-Revenga L.¹²

Affiliation:

1. Biochemistry and Molecular Genetics Department, Hospital Clinic; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS); Barcelona Spain

2. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER); Instituto de Salud Carlos III; Madrid Spain

Funder

Instituto de Salud Carlos III

Federación Española de Enfermedades Raras

Generalitat de Catalunya

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13075/fullpdf

Reference82 articles.

1. A pedigree of mental defect showing sex-linkage;Martin;J Neurol Psychiatry,1943

2. A marker X chromosome;Lubs;Am J Hum Genet,1969

3. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberlé;Science,1991

4. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991

5. Fragile X genotype characterized by an unstable region of DNA;Yu;Science,1991

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