X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.
Han G. Brunner(Radboud University Nijmegen), Bernard A. van Oost(Radboud University Nijmegen), Erik Ch. Wolters, Peter van Zandvoort, N.G.G.M. Abeling, Michaël Kuiper(Medisch Centrum Leeuwarden), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), A. H. van Gennip(Amsterdam UMC Location University of Amsterdam), Marcel Nelen(Radboud University Nijmegen)
PubMed
June 1, 1993
Cited by 369
Related Papers
Targeted Temperature Management at 33°C versus 36°C after Cardiac Arrest
|New England Journal of Medicine|2013|2.8k
Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A
|Science|1993|1.6k
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
|The American Journal of Human Genetics|2004|760
Localization of the gene for Cowden disease to chromosome 10q22–23
|Nature Genetics|1996|670