Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

172 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Clinical and molecular implications of mosaicism in FMR1 full mutations.
Pretto D, Yrigollen CM, Tang HT, Williamson J, Espinal G, Iwahashi CK, Durbin-Johnson B, Hagerman RJ, Hagerman PJ, Tassone F. Pretto D, et al. Among authors: tang ht. Front Genet. 2014 Sep 17;5:318. doi: 10.3389/fgene.2014.00318. eCollection 2014. Front Genet. 2014. PMID: 25278957 Free PMC article.
Assessment of Molecular Measures in Non-FXTAS Male Premutation Carriers.
Al Olaby RR, Tang HT, Durbin-Johnson B, Schneider A, Hessl D, Rivera SM, Tassone F. Al Olaby RR, et al. Among authors: tang ht. Front Genet. 2018 Aug 22;9:302. doi: 10.3389/fgene.2018.00302. eCollection 2018. Front Genet. 2018. PMID: 30186307 Free PMC article.
Clinical and molecular correlates in fragile X premutation females.
Jiraanont P, Sweha SR, AlOlaby RR, Silva M, Tang HT, Durbin-Johnson B, Schneider A, Espinal GM, Hagerman PJ, Rivera SM, Hessl D, Hagerman RJ, Chutabhakdikul N, Tassone F. Jiraanont P, et al. Among authors: tang ht. eNeurologicalSci. 2017 Jun;7:49-56. doi: 10.1016/j.ensci.2017.04.003. Epub 2017 Apr 11. eNeurologicalSci. 2017. PMID: 28971146 Free PMC article.
Differential increases of specific FMR1 mRNA isoforms in premutation carriers.
Pretto DI, Eid JS, Yrigollen CM, Tang HT, Loomis EW, Raske C, Durbin-Johnson B, Hagerman PJ, Tassone F. Pretto DI, et al. Among authors: tang ht. J Med Genet. 2015 Jan;52(1):42-52. doi: 10.1136/jmedgenet-2014-102593. Epub 2014 Oct 30. J Med Genet. 2015. PMID: 25358671 Free PMC article.
Size and methylation mosaicism in males with Fragile X syndrome.
Jiraanont P, Kumar M, Tang HT, Espinal G, Hagerman PJ, Hagerman RJ, Chutabhakdikul N, Tassone F. Jiraanont P, et al. Among authors: tang ht. Expert Rev Mol Diagn. 2017 Nov;17(11):1023-1032. doi: 10.1080/14737159.2017.1377612. Expert Rev Mol Diagn. 2017. PMID: 28929824 Free PMC article.
Genetic cluster of fragile X syndrome in a Colombian district.
Saldarriaga W, Forero-Forero JV, González-Teshima LY, Fandiño-Losada A, Isaza C, Tovar-Cuevas JR, Silva M, Choudhary NS, Tang HT, Aguilar-Gaxiola S, Hagerman RJ, Tassone F. Saldarriaga W, et al. Among authors: tang ht. J Hum Genet. 2018 Apr;63(4):509-516. doi: 10.1038/s10038-017-0407-6. Epub 2018 Jan 29. J Hum Genet. 2018. PMID: 29379191
172 results