Fragile X Syndrome: A Model of Gene-Brain-Behavior Relationships
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference109 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
2. Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique;Willemsen;Hum Genet,1997
3. FMRP expression as a potential prognostic indicator in fragile X syndrome;Tassone;Am J Med Genet,1999
4. Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome;Kaufmann;Am J Med Genet,1999
5. Variability in FMRP and early development in males with fragile X syndrome;Bailey;Am J Ment Retard,2001
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1. Reliability of resting-state electrophysiology in fragile X syndrome;Biomarkers in Neuropsychiatry;2023-12
2. Fragile sites, chromosomal lesions, tandem repeats, and disease;Frontiers in Genetics;2022-11-17
3. Cerebellum neuropathology and motor skill deficits in fragile X syndrome;International Journal of Developmental Neuroscience;2022-08-04
4. Uncovering Essential Tremor Genetics: The Promise of Long-Read Sequencing;Frontiers in Neurology;2022-03-23
5. Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation;Frontiers in Psychiatry;2021-10-01
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