Molecular and cellular genetics of fragile X syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference136 articles.
1. Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain
2. The neurobiology of fragile X syndrome
3. Molecular-neurobehavioral associations in females with the fragile X full mutation
4. 1998.FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome. Am J Med Genet (in press).
5. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeat
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1. Genomic hotspots of chromosome rearrangements explain conserved synteny despite high rates of chromosome evolution in a holocentric lineage;Molecular Ecology;2023-07-24
2. Size matters: Fighting repeat expansion size in fragile X syndrome using antisense oligonucleotides;Proceedings of the National Academy of Sciences;2023-07-13
3. Fragile X Messenger Ribonucleoprotein 1 (FMR1), a novel inhibitor of osteoblast/osteocyte differentiation, regulates bone formation, mass, and strength in young and aged male and female mice;Bone Research;2023-05-17
4. Communication in fragile X syndrome: Patterns and implications for assessment and intervention;Frontiers in Psychology;2022-12-22
5. Case Reports of Aortic Aneurism in Fragile X Syndrome;Genes;2022-08-30
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