High-resolution methylation polymerase chain reaction for fragile X analysis: Evidence for novel FMR1 methylation patterns undetected in Southern blot analyses

An Information-Rich CGG Repeat Primed PCR That Detects the Full Range of Fragile X Expanded Alleles and Minimizes the Need for Southern Blot Analysis

(2010) Liangjing Chen et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA

(2009) Bradford Coffee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Methyl-CpG-Binding PCR of Bloodspots for Confirmation of Fragile X Syndrome in Males

(2009) Ching-Cherng Tzeng et al.   JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY

Testing for Fragile X Gene Mutations Throughout the Life Span

(2008) Randi J. Hagerman   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Methylation-Specific Multiplex Ligation-Dependent Probe Amplification Enables a Rapid and Reliable Distinction between Male FMR1 Premutation and Full-Mutation Alleles

(2008) Anders O.H. Nygren et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Errors in the bisulfite conversion of DNA: modulating inappropriate- and failed-conversion frequencies

(2008) D. P. Genereux et al.   NUCLEIC ACIDS RESEARCH

A Rapid Polymerase Chain Reaction-Based Screening Method for Identification of All Expanded Alleles of the Fragile X (FMR1) Gene in Newborn and High-Risk Populations

(2007) Flora Tassone et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Consensus Characterization of 16 FMR1 Reference Materials: A Consortium Study

(2007) Jean Amos Wilson et al.   JOURNAL OF MOLECULAR DIAGNOSTICS