Brown WT - Search Results

1

Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate.

Gavin M, Wen GY, Messing J, Adelman S, Logush A, Jenkins EC, Brown WT, Velinov M. Gavin M, et al. Among authors: brown wt. JIMD Rep. 2013;11:87-92. doi: 10.1007/8904_2013_226. Epub 2013 Apr 16. JIMD Rep. 2013. PMID: 23588842 Free PMC article.

2

Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families.

Velinov M, Dolzhanskaya N, Gonzalez M, Powell E, Konidari I, Hulme W, Staropoli JF, Xin W, Wen GY, Barone R, Coppel SH, Sims K, Brown WT, Züchner S. Velinov M, et al. Among authors: brown wt. PLoS One. 2012;7(1):e29729. doi: 10.1371/journal.pone.0029729. Epub 2012 Jan 3. PLoS One. 2012. PMID: 22235333 Free PMC article.

3

The fragile X syndrome.

Brown WT, Jenkins EC. Brown WT, et al. Mol Genet Med. 1992;2:39-66. doi: 10.1016/b978-0-12-462002-5.50007-8. Mol Genet Med. 1992. PMID: 1458226 Review. No abstract available.

4

Transmission electron microscopy of chromosomes by longitudinal section preparation: application to fragile X chromosome analysis.

Wen GY, Jenkins EC, Yao XL, Yoon D, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: brown wt. Am J Med Genet. 1997 Feb 11;68(4):445-9. doi: 10.1002/(sici)1096-8628(19970211)68:4<445::aid-ajmg14>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9021019

5

Ultrastructure of the fragile X chromosome: new observations on the fragile site.

Wen GY, Jenkins EC, Goldberg EM, Genovese M, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: brown wt. Am J Med Genet. 1999 Apr 2;83(4):331-3. Am J Med Genet. 1999. PMID: 10208174

6

The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.

Velinov M, Gu H, Genovese M, Duncan C, Brown WT, Jenkins E. Velinov M, et al. Among authors: brown wt. Mol Genet Metab. 2000 Jan;69(1):81-3. doi: 10.1006/mgme.1999.2941. Mol Genet Metab. 2000. PMID: 10655162

7

Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses.

Zhong NA, Wisniewski KE, Ju W, Moroziewicz DN, Jurkiewicz A, McLendon L, Jenkins EC, Brown WT. Zhong NA, et al. Among authors: brown wt. Genet Test. 2000;4(3):243-8. doi: 10.1089/10906570050501452. Genet Test. 2000. PMID: 11142754

8

Human chromatid ultrastructure: new observations with scanning and transmission electron microscopy.

Jenkins EC, Wen GY, Jenkins EC Jr, Genovese M, Brown WT. Jenkins EC, et al. Among authors: brown wt. Scanning. 2002 Mar-Apr;24(2):55-8. doi: 10.1002/sca.4950240201. Scanning. 2002. PMID: 12004804

9

Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene.

Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Jenkins EC, et al. Among authors: brown wt. Am J Med Genet A. 2008 Jun 15;146A(12):1543-6. doi: 10.1002/ajmg.a.32342. Am J Med Genet A. 2008. PMID: 18478592 Free PMC article.

10

Folate receptor autoantibodies are prevalent in children diagnosed with autism spectrum disorder, their normal siblings and parents.

Quadros EV, Sequeira JM, Brown WT, Mevs C, Marchi E, Flory M, Jenkins EC, Velinov MT, Cohen IL. Quadros EV, et al. Among authors: brown wt. Autism Res. 2018 May;11(5):707-712. doi: 10.1002/aur.1934. Epub 2018 Feb 2. Autism Res. 2018. PMID: 29394471

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