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

5 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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: riddle je. 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
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. 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
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. 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