Epidemiology of fragile X syndrome: A systematic review and meta-analysis

Prevalence of CGG expansions of the FMR1 gene in a US population-based sample

(2012) Marsha Mailick Seltzer et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Fragile X Syndrome

(2012) Yingratana McLennan et al.   CURRENT GENOMICS

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics

(2012) Claudia Bagni et al.   JOURNAL OF CLINICAL INVESTIGATION

Health and Economic Consequences of Fragile X Syndrome for Caregivers

(2012) Donald B. Bailey et al.   JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS

The neurochemical basis for the treatment of autism spectrum disorders and Fragile X Syndrome

(2011) David R. Hampson et al.   BIOCHEMICAL PHARMACOLOGY

A New Method for FMR1 Gene Methylation Screening by Multiplex Methylation-Specific Real-Time Polymerase Chain Reaction

(2011) Marjanu Hikmah Elias et al.   Genetic Testing and Molecular Biomarkers

Fragile X CGG Repeat Variation in Tamil Nadu, South India: A Comparison of Radioactive and Methylation-Specific Polymerase Chain Reaction in CGG Repeat Sizing

(2011) Nagarathinam Indhumathi et al.   Genetic Testing and Molecular Biomarkers

Targeted treatments for fragile X syndrome

(2011) Elizabeth Berry-Kravis et al.   Journal of Neurodevelopmental Disorders

Therapeutic Strategies in Fragile X Syndrome: Dysregulated mGluR Signaling and Beyond

(2011) Christina Gross et al.   NEUROPSYCHOPHARMACOLOGY

Toward Fulfilling the Promise of Molecular Medicine in Fragile X Syndrome

(2010) Dilja D. Krueger et al.   Annual Review of Medicine

Frequency of fragile X chromosome in normal females

(2010) Dunne Abuelo et al.   CLINICAL GENETICS

Applicability of a checklist for clinical screening of the fragile X syndrome

(2010) M. Arvio et al.   CLINICAL GENETICS

Fragile X syndrome in mildly mentally retarded children in a Northern Swedish county. A prevalence study

(2010) H. Kson Blomquist et al.   CLINICAL GENETICS

An epidemiological/genetic study of mental subnormality in Assiut Governorate, Egypt

(2010) S. A. Temtamy et al.   CLINICAL GENETICS

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States

(2010) Feras M Hantash et al.   GENETICS IN MEDICINE

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio

(2010) David Eugeny Godler et al.   HUMAN MOLECULAR GENETICS

A Unified Rapid PCR Method for Detection of Normal and Expanded Trinucleotide Alleles of CAG Repeats in Huntington Chorea and CGG Repeats in Fragile X Syndrome

(2010) Tihomir Todorov et al.   MOLECULAR BIOTECHNOLOGY

Committee Opinion No. 469: Carrier Screening for Fragile X Syndrome

(2010)   OBSTETRICS AND GYNECOLOGY

Potential therapeutic interventions for fragile X syndrome

(2010) Josien Levenga et al.   TRENDS IN MOLECULAR MEDICINE

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

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

Fragile X carrier screening and FMR1 allele distribution in the Japanese population

(2009) Susumu Otsuka et al.   BRAIN & DEVELOPMENT

Screening and instability ofFMR1alleles in a prospective sample of 24,449 mother–newborn pairs from the general population

(2009) S Lévesque et al.   CLINICAL GENETICS

Expansion of an FMR1 Grey-Zone Allele to a Full Mutation in Two Generations

(2009) Isabel Fernandez-Carvajal et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Screening for Expanded Alleles of the FMR1 Gene in Blood Spots from Newborn Males in a Spanish Population

(2009) Isabel Fernandez-Carvajal et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Molecular diagnosis of Fragile X syndrome

(2008) Christalena Sofocleous et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Prevalence of the Fragile X Syndrome Among Estonian Mentally Retarded and the Entire Children's Population

(2008) Helen Puusepp et al.   JOURNAL OF CHILD NEUROLOGY

Primary ovarian insufficiency: a more accurate term for premature ovarian failure

(2007) Corrine K. Welt   CLINICAL ENDOCRINOLOGY

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