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591 results

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Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X.
Loesch DZ, Bui QM, Dissanayake C, Clifford S, Gould E, Bulhak-Paterson D, Tassone F, Taylor AK, Hessl D, Hagerman R, Huggins RM. Loesch DZ, et al. Among authors: hagerman r. Neurosci Biobehav Rev. 2007;31(3):315-26. doi: 10.1016/j.neubiorev.2006.09.007. Epub 2006 Nov 9. Neurosci Biobehav Rev. 2007. PMID: 17097142 Free PMC article. 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
Molecular/clinical correlations in females with fragile X.
Sobesky WE, Taylor AK, Pennington BF, Bennetto L, Porter D, Riddle J, Hagerman RJ. Sobesky WE, et al. Among authors: hagerman rj. Am J Med Genet. 1996 Aug 9;64(2):340-5. doi: 10.1002/(SICI)1096-8628(19960809)64:2<340::AID-AJMG21>3.0.CO;2-E. Am J Med Genet. 1996. PMID: 8844077
Molecular-clinical correlations in males with an expanded FMR1 mutation.
Merenstein SA, Sobesky WE, Taylor AK, Riddle JE, Tran HX, Hagerman RJ. Merenstein SA, et al. Among authors: hagerman rj. Am J Med Genet. 1996 Aug 9;64(2):388-94. doi: 10.1002/(SICI)1096-8628(19960809)64:2<388::AID-AJMG31>3.0.CO;2-9. Am J Med Genet. 1996. PMID: 8844089
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
591 results