Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation

This publication has 69 references indexed in Scilit:

• Characterization of Potocki-Lupski Syndrome (dup(17)(p11.2p11.2)) and Delineation of a Dosage-Sensitive Critical Interval That Can Convey an Autism Phenotype
  American Journal of Human Genetics, 2007
• Genome-wide Copy Number Profiling on High-density Bacterial Artificial Chromosomes, Single-nucleotide Polymorphisms, and Oligonucleotide Microarrays: A Platform Comparison based on Statistical Power Analysis
  DNA Research, 2007
• High resolution array-CGH analysis of single cells
  Nucleic Acids Research, 2006
• Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
  Nature Genetics, 2006
• Global variation in copy number in the human genome
  Nature, 2006
• Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
  Genome Research, 2006
• Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation
  American Journal of Human Genetics, 2006
• High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping
  Genome Research, 2006
• BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)
  Nucleic Acids Research, 2006
• Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness
  European Journal of Human Genetics, 2004