Hagerman RJ - Search Results

1

Utari A, Adams E, Berry-Kravis E, Chavez A, Scaggs F, Ngotran L, Boyd A, Hessl D, Gane LW, Tassone F, Tartaglia N, Leehey MA, Hagerman RJ. Utari A, et al. Among authors: hagerman rj. J Neurodev Disord. 2010 Jun;2(2):70-76. doi: 10.1007/s11689-010-9047-2. Epub 2010 May 12. J Neurodev Disord. 2010. PMID: 20585378 Free PMC article.

2

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

3

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

4

Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome.

Taylor AK, Tassone F, Dyer PN, Hersch SM, Harris JB, Greenough WT, Hagerman RJ. Taylor AK, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):233-9. Am J Med Genet. 1999. PMID: 10331599

5

Tassone F, Hagerman RJ, Gane LW, Taylor AK. Tassone F, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):240-4. Am J Med Genet. 1999. PMID: 10331600

6

FMRP expression as a potential prognostic indicator in fragile X syndrome.

Tassone F, Hagerman RJ, Iklé DN, Dyer PN, Lampe M, Willemsen R, Oostra BA, Taylor AK. Tassone F, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):250-61. Am J Med Genet. 1999. PMID: 10331602

7

Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development.

Freedenberg DL, Gane LW, Richards CS, Lampe M, Hills J, O'Connor R, Manchester D, Taylor A, Tassone F, Hulseberg D, Hagerman RJ, Patil SR. Freedenberg DL, et al. Among authors: hagerman rj. Am J Med Genet. 1999 Jul 30;85(3):197-201. doi: 10.1002/(sici)1096-8628(19990730)85:3<197::aid-ajmg1>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10398226

8

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Hum Genet. 2000 Jan;66(1):6-15. doi: 10.1086/302720. Am J Hum Genet. 2000. PMID: 10631132 Free PMC article.

9

Clinical involvement and protein expression in individuals with the FMR1 premutation.

Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Mar 13;91(2):144-52. doi: 10.1002/(sici)1096-8628(20000313)91:2<144::aid-ajmg14>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10748416

10

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

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