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Progression of tremor and ataxia in male carriers of the FMR1 premutation.
Leehey MA, Berry-Kravis E, Min SJ, Hall DA, Rice CD, Zhang L, Grigsby J, Greco CM, Reynolds A, Lara R, Cogswell J, Jacquemont S, Hessl DR, Tassone F, Hagerman R, Hagerman PJ. Leehey MA, et al. Among authors: hagerman pj, hagerman r. Mov Disord. 2007 Jan 15;22(2):203-6. doi: 10.1002/mds.21252. Mov Disord. 2007. PMID: 17133502
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.
Fragile X syndrome in a normal IQ male with learning and emotional problems.
Merenstein SA, Shyu V, Sobesky WE, Staley L, Berry-Kravis E, Nelson DL, Lugenbeel KA, Taylor AK, Pennington BF, Hagerman RJ. Merenstein SA, et al. Among authors: hagerman rj. J Am Acad Child Adolesc Psychiatry. 1994 Nov-Dec;33(9):1316-21. doi: 10.1097/00004583-199411000-00014. J Am Acad Child Adolesc Psychiatry. 1994. PMID: 7995799
Phenotypic involvement in females with the FMR1 gene mutation.
Riddle JE, Cheema A, Sobesky WE, Gardner SC, Taylor AK, Pennington BF, Hagerman RJ. Riddle JE, et al. Among authors: hagerman rj. Am J Ment Retard. 1998 May;102(6):590-601. doi: 10.1352/0895-8017(1998)102<0590:piifwt>2.0.co;2. Am J Ment Retard. 1998. PMID: 9606468
Compound heterozygous female with fragile X syndrome.
Linden MG, Tassone F, Gane LW, Hills JL, Hagerman RJ, Taylor AK. Linden MG, et al. Among authors: hagerman rj. Am J Med Genet. 1999 Apr 2;83(4):318-21. Am J Med Genet. 1999. PMID: 10208169
602 results