Obstetrical and gynecological complications in fragile X carriers: A multicenter study
Charles E. Schwartz(Greenwood Genetic Center), Roger E. Stevenson(Piedmont Technical College), Randi J. Hagerman(University of California Davis Medical Center), Claire Hull(Children's Hospital Colorado), Margareta Mikkelsen(Kennedy Center), M. Bugge(Kennedy Center), Jeanette J. A. Holden, Patricia N. Howard‐Peebles(Genetics and IVF Institute), Jane H. Dean(Greenwood Genetic Center), Niels Tommerup(University of Copenhagen)
Cited by 205
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
<i>AGTR2</i> Mutations in X-Linked Mental Retardation
|Science|2002|719
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
|Nature Genetics|2008|591
X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene
|Nature Genetics|1994|420
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes
|Proceedings of the National Academy of Sciences|2004|420