Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
Reinhard Ullmann(Max Planck Institute for Molecular Genetics), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), Ines Müller(Max Planck Institute for Molecular Genetics), Lynn Banna(John Hunter Hospital), Avril V. Brereton(Monash University), Carla Rosenberg(Universidade de São Paulo), Gillian Turner(Hunter Genetics), Claus Hultschig(Max Planck Institute for Molecular Genetics), Michael Field(Hunter Genetics), Alyssa C. Hill(ETH Zurich), Ana Cristina Victorino Krepischi(Universidade de São Paulo), Georg Wieczorek(Max Planck Institute for Molecular Genetics), Fikret Erdogan(Max Planck Institute for Molecular Genetics), Angela Maria Vianna‐Morgante(Universidade de São Paulo), Bruce J. Tonge(Monash University), Maria Kirchhoff(Rigshospitalet), Louise Christie(Hunter Genetics), Wei Chen(Southern University of Science and Technology), Anne‐Marie Bisgaard(Rigshospitalet)
Cited by 288
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