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■ Abbreviation / Long Form : CGG / cytosine-guanine-guanine

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Total Number of Papers: 24
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Abbreviation:   CGG  (>> Co-occurring Abbreviation)
Long Form:   cytosine-guanine-guanine
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No. Year Title Co-occurring Abbreviation
2019 A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene. FMR1, FXS, PCR, UTR
2019 Fragile X syndrome in a male with methylated premutation alleles and no detectable methylated full mutation alleles. FM, FXS, PM
2019 New Targeted Treatments in Fragile X Syndrome. FMR1, FMRP, FXS
2019 Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing. FM, FXS, PM
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
10  2016 [Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family]. FXS
11  2015 Cascade Screening for Fragile X Syndrome/CGG Repeat Expansions in Children Attending Special Education in Sri Lanka. FXS
12  2015 Evidence of an age-related correlation of ovarian reserve and FMR1 repeat number among women with "normal" CGG repeat status. AMH, FMR1, PM
13  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
14  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
15  2014 Visual motion processing deficits in infants with the fragile X premutation. DS, FMRP, FX, FXS, TD
16  2012 Fragile X-associated disorders: a clinical overview. FraX
17  2009 Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India. FMR1
18  2004 A neuropsychological investigation of male premutation carriers of fragile X syndrome. ---
19  2001 An assessment of screening strategies for fragile X syndrome in the UK. ---
20  2001 [From gene to disease; fragile X-syndrome: hereditary mental retardation due to a developmental gene]. ---
21  2000 A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: a preliminary report. ---
22  1997 The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis. CAG, CTG
23  1993 A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome. FMR1
24  1993 Molecular-clinical correlations in children and adults with fragile X syndrome. FMR1