Identification and molecular characterization of two novel chromosomal deletions associated with autism

Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature

(2009) Michael R. Rossi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

(2009) Margaret J. Wat et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders

(2009) HM Ozgen et al.   CLINICAL GENETICS

Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder

(2009) I. Cusco et al.   HUMAN MOLECULAR GENETICS

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

(2008) Susan L. Christian et al.   BIOLOGICAL PSYCHIATRY

A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan

(2008) Chien-Hsing Lin et al.   BMC GENETICS

A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia

(2008) Mette Gilling et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Defensins and the dynamic genome: What we can learn from structural variation at human chromosome band 8p23.1

(2008) E. J. Hollox et al.   GENOME RESEARCH

Advances in autism genetics: on the threshold of a new neurobiology

(2008) Brett S. Abrahams et al.   NATURE REVIEWS GENETICS

Association between Microdeletion and Microduplication at 16p11.2 and Autism

(2008) Lauren A. Weiss et al.   NEW ENGLAND JOURNAL OF MEDICINE