High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome

Lan K. Hornstra(University of Florida), Thomas P. Yang(China Agricultural University), David L. Nelson(Baylor College of Medicine), Stephen T. Warren(Emory University)
Human Molecular Genetics
January 1, 1993
10.1093/hmg/2.10.1659
Cited by 128

Related Papers

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
|Cell|1991|3.5k
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
|Cell|1991|2.1k
Absence of expression of the FMR-1 gene in fragile X syndrome
|Cell|1991|1.5k
Folate and DNA Methylation: A Review of Molecular Mechanisms and the Evidence for Folate's Role
|Advances in Nutrition|2012|989
Novel 10-kHz High-frequency Therapy (HF10 Therapy) Is Superior to Traditional Low-frequency Spinal Cord Stimulation for the Treatment of Chronic Back and Leg Pain
|Anesthesiology|2015|828