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

This publication has 39 references indexed in Scilit:

• Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
  American Journal of Human Genetics, 2010
• High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
  European Journal of Human Genetics, 2009
• Clinical Utility of Array Comparative Genomic Hybridization: Uncovering Tumor Susceptibility in Individuals with Developmental Delay
  The Journal of Pediatrics, 2009
• Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization
  BMC Genomics, 2009
• Disruption of the neurexin 1 gene is associated with schizophrenia
  Human Molecular Genetics, 2008
• Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
  Molecular Cytogenetics, 2008
• Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
  Biological Psychiatry, 2008
• Disruption of contactin 4 in three subjects with autism spectrum disorder
  Journal of Medical Genetics, 2008
• Strong Association of De Novo Copy Number Mutations with Autism
  Science, 2007
• Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases
  PLOS ONE, 2007