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

745 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
Tarpey PS, Raymond FL, O'Meara S, Edkins S, Teague J, Butler A, Dicks E, Stevens C, Tofts C, Avis T, Barthorpe S, Buck G, Cole J, Gray K, Halliday K, Harrison R, Hills K, Jenkinson A, Jones D, Menzies A, Mironenko T, Perry J, Raine K, Richardson D, Shepherd R, Small A, Varian J, West S, Widaa S, Mallya U, Moon J, Luo Y, Holder S, Smithson SF, Hurst JA, Clayton-Smith J, Kerr B, Boyle J, Shaw M, Vandeleur L, Rodriguez J, Slaugh R, Easton DF, Wooster R, Bobrow M, Srivastava AK, Stevenson RE, Schwartz CE, Turner G, Gecz J, Futreal PA, Stratton MR, Partington M. Tarpey PS, et al. Among authors: kerr b. Am J Hum Genet. 2007 Feb;80(2):345-52. doi: 10.1086/511134. Epub 2007 Jan 4. Am J Hum Genet. 2007. PMID: 17236139 Free PMC article.
Nomenclature guidelines for X-linked mental retardation.
Mulley JC, Kerr B, Stevenson R, Lubs H. Mulley JC, et al. Among authors: kerr b. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):383-91. doi: 10.1002/ajmg.1320430159. Am J Med Genet. 1992. PMID: 1605216 Review.
Smith-Fineman-Myers syndrome in two brothers.
Adès LC, Kerr B, Turner G, Wise G. Adès LC, et al. Among authors: kerr b. Am J Med Genet. 1991 Sep 15;40(4):467-70. doi: 10.1002/ajmg.1320400419. Am J Med Genet. 1991. PMID: 1684092
Non-specific X linked mental retardation.
Kerr B, Turner G, Mulley J, Gedeon A, Partington M. Kerr B, et al. J Med Genet. 1991 Jun;28(6):378-82. doi: 10.1136/jmg.28.6.378. J Med Genet. 1991. PMID: 1870094 Free PMC article. Review.
How many X-linked genes for non-specific mental retardation (MRX) are there?
Gedeon AK, Donnelly AJ, Mulley JC, Kerr B, Turner G. Gedeon AK, et al. Among authors: kerr b. Am J Med Genet. 1996 Jul 12;64(1):158-62. doi: 10.1002/(SICI)1096-8628(19960712)64:1<158::AID-AJMG26>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8826466 Review. No abstract available.
745 results