A family with the Coffin Lowry syndrome revisited: Localization of CLS to Xp21‐pter
M. W. Partington(University of King's College), Gillian Turner(Hunter Genetics), A. Thode(Prince of Wales Hospital), J.C. Mulley, G.R. Sutherland(Women's and Children's Hospital)
Cited by 39
Related Papers
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
|Human Genetics|1985|512
PAK3 mutation in nonsyndromic X-linked mental retardation
|Nature Genetics|1998|472
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
|Nature Genetics|2002|437
Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
|The American Journal of Human Genetics|2005|376