Taylor AK - Search Results

1

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. Am J Med Genet. 1999 May 28;84(3):233-9. Am J Med Genet. 1999. PMID: 10331599

2

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. 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

3

Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.

Taylor AK, Safanda JF, Fall MZ, Quince C, Lang KA, Hull CE, Carpenter I, Staley LW, Hagerman RJ. Taylor AK, et al. JAMA. 1994 Feb 16;271(7):507-14. JAMA. 1994. PMID: 8301764

4

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: taylor ak. 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

5

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: taylor ak. 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

6

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: taylor ak. 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

7

Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report.

Miller LJ, McIntosh DN, McGrath J, Shyu V, Lampe M, Taylor AK, Tassone F, Neitzel K, Stackhouse T, Hagerman RJ. Miller LJ, et al. Among authors: taylor ak. Am J Med Genet. 1999 Apr 2;83(4):268-79. Am J Med Genet. 1999. PMID: 10208160

8

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: taylor ak. Am J Med Genet. 1999 Apr 2;83(4):318-21. Am J Med Genet. 1999. PMID: 10208169

9

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

10

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: taylor ak. Am J Med Genet. 1999 May 28;84(3):250-61. Am J Med Genet. 1999. PMID: 10331602

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