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Fragile X protein in newborn dried blood spots.
Adayev T, LaFauci G, Dobkin C, Caggana M, Wiley V, Field M, Wotton T, Kascsak R, Nolin SL, Glicksman A, Hosmer N, Brown WT. Adayev T, et al. Among authors: brown wt. BMC Med Genet. 2014 Oct 28;15:119. doi: 10.1186/s12881-014-0119-0. BMC Med Genet. 2014. PMID: 25348928 Free PMC article.
The role of reduced expression of fragile X mental retardation protein in neurons and increased expression in astrocytes in idiopathic and syndromic autism (duplications 15q11.2-q13).
Wegiel J, Brown WT, La Fauci G, Adayev T, Kascsak R, Kascsak R, Flory M, Kaczmarski W, Kuchna I, Nowicki K, Martinez-Cerdeno V, Wisniewski T, Wegiel J. Wegiel J, et al. Among authors: brown wt. Autism Res. 2018 Oct;11(10):1316-1331. doi: 10.1002/aur.2003. Epub 2018 Aug 14. Autism Res. 2018. PMID: 30107092
A Genotype-Phenotype Study of High-Resolution FMR1 Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments.
Budimirovic DB, Schlageter A, Filipovic-Sadic S, Protic DD, Bram E, Mahone EM, Nicholson K, Culp K, Javanmardi K, Kemppainen J, Hadd A, Sharp K, Adayev T, LaFauci G, Dobkin C, Zhou L, Brown WT, Berry-Kravis E, Kaufmann WE, Latham GJ. Budimirovic DB, et al. Among authors: brown wt. Brain Sci. 2020 Sep 30;10(10):694. doi: 10.3390/brainsci10100694. Brain Sci. 2020. PMID: 33008014 Free PMC article.
Prospects for gene therapy in the fragile X syndrome.
Rattazzi MC, LaFauci G, Brown WT. Rattazzi MC, et al. Among authors: brown wt. Ment Retard Dev Disabil Res Rev. 2004;10(1):75-81. doi: 10.1002/mrdd.20012. Ment Retard Dev Disabil Res Rev. 2004. PMID: 14994292 Review.
Clinical aspects of the fragile X syndrome.
Brown WT. Brown WT. Results Probl Cell Differ. 2012;54:273-9. doi: 10.1007/978-3-642-21649-7_15. Results Probl Cell Differ. 2012. PMID: 22009358
397 results