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Adaptive, behavioral, and cognitive outcomes in individuals with fragile X syndrome with varying autism severity.
Aishworiya R, Tak YE, Ponzini MD, Biag HMB, Salcedo-Arellano MJ, Kim K, Tassone F, Schneider A, Thurman AJ, Abbeduto L, Hessl D, Randol JL, Bolduc FV, Lippe S, Hagerman P, Hagerman R. Aishworiya R, et al. Among authors: hagerman p. Int J Dev Neurosci. 2023 Dec;83(8):715-727. doi: 10.1002/jdn.10299. Epub 2023 Sep 19. Int J Dev Neurosci. 2023. PMID: 37724826 Free PMC article.
The fragile X syndrome: history, diagnosis, and treatment.
Hagerman RJ, McBogg P, Hagerman PJ. Hagerman RJ, et al. Among authors: hagerman pj. J Dev Behav Pediatr. 1983 Jun;4(2):122-30. doi: 10.1097/00004703-198306000-00009. J Dev Behav Pediatr. 1983. PMID: 6348096 Review.
Transcription of the FMR1 gene in individuals with fragile X syndrome.
Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Fall;97(3):195-203. doi: 10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R. Am J Med Genet. 2000. PMID: 11449488
The fragile X premutation: into the phenotypic fold.
Hagerman RJ, Hagerman PJ. Hagerman RJ, et al. Curr Opin Genet Dev. 2002 Jun;12(3):278-83. doi: 10.1016/s0959-437x(02)00299-x. Curr Opin Genet Dev. 2002. PMID: 12076670 Review.
260 results