Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

@article{Miller2010ConsensusSC,
  title={Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.},
  author={D. Miller and M. Adam and S. Aradhya and L. Biesecker and A. Brothman and N. Carter and D. Church and J. Crolla and E. Eichler and C. Epstein and W. A. Faucett and L. Feuk and J. Friedman and A. Hamosh and L. Jackson and E. B. Kaminsky and K. Kok and I. Krantz and R. M. Kuhn and C. Lee and J. Ostell and C. Rosenberg and S. Scherer and N. Spinner and D. J. Stavropoulos and J. Tepperberg and E. Thorland and J. Vermeesch and D. Waggoner and M. Watson and C. Martin and D. H. Ledbetter},
  journal={American journal of human genetics},
  year={2010},
  volume={86 5},
  pages={
          749-64
        }
}
  • D. Miller, M. Adam, +29 authors D. H. Ledbetter
  • Published 2010
  • Biology, Medicine
  • American journal of human genetics
  • Chromosomal microarray (CMA) is increasingly utilized for genetic testing of individuals with unexplained developmental delay/intellectual disability (DD/ID), autism spectrum disorders (ASD), or multiple congenital anomalies (MCA). Performing CMA and G-banded karyotyping on every patient substantially increases the total cost of genetic testing. The International Standard Cytogenomic Array (ISCA) Consortium held two international workshops and conducted a literature review of 33 studies… CONTINUE READING
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