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Descriptive analysis of seizures and comorbidities associated with fragile X syndrome.
Albizua I, Charen K, Shubeck L, Talboy A, Berry-Kravis E, Kaufmann WE, Stallworth JL, Drazba KT, Erickson CA, Sweeney JA, Tartaglia N, Warren SF, Hagerman R, Sherman SL, Warren ST, Jin P, Allen EG. Albizua I, et al. Among authors: warren st. Mol Genet Genomic Med. 2022 Aug;10(8):e2001. doi: 10.1002/mgg3.2001. Epub 2022 Jul 18. Mol Genet Genomic Med. 2022. PMID: 35852003 Free PMC article.
Human genes containing polymorphic trinucleotide repeats.
Riggins GJ, Lokey LK, Chastain JL, Leiner HA, Sherman SL, Wilkinson KD, Warren ST. Riggins GJ, et al. Among authors: warren st. Nat Genet. 1992 Nov;2(3):186-91. doi: 10.1038/ng1192-186. Nat Genet. 1992. PMID: 1345166
The fragile X syndrome: no evidence for any recent mutations.
Smits AP, Dreesen JC, Post JG, Smeets DF, de Die-Smulders C, Spaans-van der Bijl T, Govaerts LC, Warren ST, Oostra BA, van Oost BA. Smits AP, et al. Among authors: warren st. J Med Genet. 1993 Feb;30(2):94-6. doi: 10.1136/jmg.30.2.94. J Med Genet. 1993. PMID: 8445628 Free PMC article.
Trinucleotide repetition and fragile X syndrome.
Warren ST. Warren ST. Hosp Pract (1995). 1997 Apr 15;32(4):73-6, 81-5, 90-2 passim. doi: 10.1080/21548331.1997.11443466. Hosp Pract (1995). 1997. PMID: 9109809 Review.
215 results