Sage Journals: Discover world-class research

Retricted access

Brief report

First published 2001-06

Compound Heterozygosity at the FMR1 Gene

Madhuri R. Hegde, Matthew Fawkner, Belinda Chong [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2009-05

Can the FMR1 (Fragile X) Gene Serve As Predictor of Response to Ovarian Stimulation?

Norbert Gleicher, Andrea Weghofer, Kutluk Oktay [...]

Reproductive Sciences

Retricted access

Research article

First published 2012-03

Identification of Expanded Alleles of the FMR1 Gene Among High-Risk Population in Indonesia by Using Blood Spot Screening

Tri Indah Winarni, Agustini Utari, Farmaditya E.P. Mundhofir [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2003-12

FMR1 Gene Deletion/Reversion: A Pitfall of Fragile X Carrier Testing

M. Gasteiger, E. Grasbon-Frodl, B. Neitzel [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2011-04

Distribution of CGG/GCC Repeats at the FMR1 and FMR2 Genes in an Indian Population with Mental Retardation of Unknown Etiology

Lavanya Katikala, Mallikarjuna R. Guruju, Sujatha Madireddi [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2011-06

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

Marjanu Hikmah Elias, Ravindran Ankathil, Abdul Razak Salmi [...]

Genetic Testing and Molecular Biomarkers

Free access

Editorial

First published 2010-3

Can the FMR1 Gene Predict Early Ovarian Aging?

Norbert Gleiche, David H Barad

Women's Health

Open access

Case report

First published 2018-12-20

Presentation of a recurrent FMR1 missense mutation (R138Q) in an affected female

Jullianne Diaz, Cathy Scheiner, Eyby Leon

Translational Science of Rare Diseases

Retricted access

Research article

First published 2012-03

Evaluation of the Human Fragile X Mental Retardation 1 Polymerase Chain Reaction Reagents to Amplify the FMR1 Gene: Testing in a Clinical Diagnostic Laboratory

Fatimah A. Nahhas, Thomas J. Monroe, Thomas W. Prior [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Review article

First published 2012-6

Severe Hunter Syndrome (Mucopolysaccharidosis II) Phenotype Secondary to Large Deletion in the X Chromosome Encompassing IDS,FMR1,and AFF2 ( FMR2 )

Day M. Burruss, Tim C. Wood, Lesby Espinoza [...]

Journal of Child Neurology

Search results