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Abbreviation : CGG
Long Form : cytosine-guanine-guanine
No. Year Title Co-occurring Abbreviation
2018 FMR1 premutation frequency in a large, ethnically diverse population referred for carrier testing. FXS
2018 Fragile-X Syndrome Is Associated With NMDA Receptor Hypofunction and Reduced Dendritic Complexity in Mature Dentate Granule Cells. AMPA, EPSCs, Fmr1 KO, FMRP, FXS, GCL, NMDAR
2017 Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis. FMR1
2017 Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability. 5'UTR, FMR1, FXS, ms-PCR
2017 Prevalence of Fragile X Syndrome among children receiving special education and carrier states in first degree relatives. FMR1, FXS
2016 [Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family]. FXS
2015 Cascade Screening for Fragile X Syndrome/CGG Repeat Expansions in Children Attending Special Education in Sri Lanka. FXS
2015 Evidence of an age-related correlation of ovarian reserve and FMR1 repeat number among women with "normal" CGG repeat status. AMH, FMR1, PM
2014 Similar prevalence of expanded CGG repeat lengths in the fragile X mental retardation I gene among infertile women and among women with proven fertility: a prospective study. FMR1
10  2014 Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI). FMR1, FXPOI, FXS, FXTAS, RAN
11  2014 Visual motion processing deficits in infants with the fragile X premutation. DS, FMRP, FX, FXS, TD
12  2012 Fragile X-associated disorders: a clinical overview. FraX
13  2009 Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India. FMR1
14  2004 A neuropsychological investigation of male premutation carriers of fragile X syndrome. ---
15  2001 An assessment of screening strategies for fragile X syndrome in the UK. ---
16  2001 [From gene to disease; fragile X-syndrome: hereditary mental retardation due to a developmental gene]. ---
17  2000 A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: a preliminary report. ---
18  1997 The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis. CAG, CTG
19  1993 A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome. FMR1
20  1993 Molecular-clinical correlations in children and adults with fragile X syndrome. FMR1