Pages that link to "Q48841668"
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The following pages link to Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance (Q48841668):
Displaying 27 items.
- The multiple molecular facets of fragile X-associated tremor/ataxia syndrome (Q26852891) (← links)
- The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009 (Q28259199) (← links)
- CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles (Q33567772) (← links)
- Reduced excitatory amino acid transporter 1 and metabotropic glutamate receptor 5 expression in the cerebellum of fragile X mental retardation gene 1 premutation carriers with fragile X-associated tremor/ataxia syndrome (Q33775794) (← links)
- Language Development in Individuals with Fragile X Syndrome (Q33788960) (← links)
- Biomarkers in the Study of Families of Individuals with Developmental Disabilities (Q33795272) (← links)
- Associated features in females with an FMR1 premutation (Q34000722) (← links)
- Lifespan changes in working memory in fragile X premutation males (Q34154343) (← links)
- The emergence of genomic psychology. Insights from genomic analyses might allow psychologists to understand, predict and modify human behaviour (Q35891843) (← links)
- Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice (Q36626883) (← links)
- Language development and fragile X syndrome: profiles, syndrome-specificity, and within-syndrome differences. (Q36746547) (← links)
- Altered neural activity in the 'when' pathway during temporal processing in fragile X premutation carriers (Q36902952) (← links)
- Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers (Q36966615) (← links)
- The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance (Q36966622) (← links)
- Co-occurring diagnoses among FMR1 premutation allele carriers (Q36966641) (← links)
- Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms (Q36966653) (← links)
- Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature. (Q37120607) (← links)
- No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50 (Q37156229) (← links)
- Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions (Q37730919) (← links)
- FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile (Q37732459) (← links)
- Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management (Q38875623) (← links)
- Implications of the FMR1 Premutation for Children, Adolescents, Adults, and Their Families (Q40080863) (← links)
- Broad autism spectrum and obsessive-compulsive symptoms in adults with the fragile X premutation (Q40976205) (← links)
- Size and methylation mosaicism in males with Fragile X syndrome. (Q46006405) (← links)
- Clinical and molecular correlates in fragile X premutation females. (Q46017813) (← links)
- Assessment of Molecular Measures in Non-FXTAS Male Premutation Carriers (Q58719238) (← links)
- FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation (Q58801569) (← links)