<i>AGTR2</i> Mutations in X-Linked Mental RetardationVirginie Vervoort, Anand K. Srivastava, Michael A. Beachem et al.|Science|2002Cited by 719
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizuresAndrew J. Sharp, Evan E. Eichler, Heather C. Mefford et al.|Nature Genetics|2008Cited by 591
X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 geneMonique Jouet, Susan Kenwrick, John R. MacFarlane et al.|Nature Genetics|1994Cited by 420
Evaluation of mental retardation: Recommendations of a consensus conferenceCynthia J. Curry, John M. Opitz, Roger E. Stevenson et al.|American Journal of Medical Genetics|1997Cited by 403
Autism and maternally derived aberrations of chromosome 15qRichard J. Schroer, Roger E. Stevenson, Mary C. Phelan et al.|American Journal of Medical Genetics|1998Cited by 372