The Genetic Distance between the Coagulation Factor IX Gene and the Locus for the Fragile X Syndrome: Clinical Implications
Cynthia Forster‐Gibson, B. N. White(Queen's University), M. W. Partington(University of King's College), Lois M. Mulligan(Queen's University), Jeanette J. A. Holden, Nancy E. Simpson(Queen's University)
Cited by 17
Related Papers
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
|Cell|1991|2.1k
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
Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation
|The American Journal of Human Genetics|2008|223