Taylor AK - Search Results

1

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: taylor ak. 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

2

A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

Tassone F, Pan R, Amiri K, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: taylor ak. J Mol Diagn. 2008 Jan;10(1):43-9. doi: 10.2353/jmoldx.2008.070073. Epub 2007 Dec 28. J Mol Diagn. 2008. PMID: 18165273 Free PMC article.

3

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

4

Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.

Loesch DZ, Sherwell S, Kinsella G, Tassone F, Taylor A, Amor D, Sung S, Evans A. Loesch DZ, et al. Clin Genet. 2012 Jul;82(1):88-92. doi: 10.1111/j.1399-0004.2011.01675.x. Epub 2011 Apr 28. Clin Genet. 2012. PMID: 21476992

5

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

6

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

7

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

8

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

9

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

10

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

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