Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

(2010) Stuart A Scott et al.   GENETICS IN MEDICINE

Clinical Genetic Testing for Patients With Autism Spectrum Disorders

(2010) Y. Shen et al.   PEDIATRICS

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

(2009) JM Friedman et al.   BMC GENOMICS

Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability

(2009) John B Moeschler   CURRENT OPINION IN NEUROLOGY

High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?

(2009) Laura Bernardini et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

(2009) Ron Hochstenbach et al.   European Journal of Medical Genetics

How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delay

(2009) Jennifer Saam et al.   GENETICS IN MEDICINE

Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH

(2009) Sara Anne Adams et al.   GENETICS IN MEDICINE

Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay

(2008) Bixia Xiang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies

(2008) Lisa Edelmann et al.   Annals of the New York Academy of Sciences

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

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

Extending genome-wide association studies to copy-number variation

(2008) S. A. McCarroll   HUMAN MOLECULAR GENETICS

Disruption of contactin 4 in three subjects with autism spectrum disorder

(2008) J Roohi et al.   JOURNAL OF MEDICAL GENETICS

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

(2008) D T Miller et al.   JOURNAL OF MEDICAL GENETICS

Clinical Utility of Array Comparative Genomic Hybridization: Uncovering Tumor Susceptibility in Individuals with Developmental Delay

(2008) Margaret P. Adam et al.   JOURNAL OF PEDIATRICS

Genetic Evaluation of Intellectual Disabilities

(2008) John B. Moeschler   Seminars in Pediatric Neurology

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype

(2008) Carolina Sismani et al.   Molecular Cytogenetics