Genetics of intellectual disability
Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics)
Cited by 207
Related Papers
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
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
|Nature Genetics|2009|617