118
Views
0
CrossRef citations to date
0
Altmetric
General Content - Editorial

Chromosomal Microarrays: Influential Players in the Diagnosis of Developmental Disorders

, &
Pages 167-169 | Published online: 06 Mar 2012

References

  • Hochstenbach R , van BinsbergenE, EngelenJet al. Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in The Netherlands. Eur. J. Med. Genet.52(4), 161–169 (2009).
  • Miller DT , AdamMP, AradhyaSet al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am. J. Hum. Genet.86(5), 749–764 (2010).
  • Rauch A , HoyerJ, GuthSet al. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. Am. J. Med. Genet. A140(19), 2063–2074 (2006).
  • Sebat J , LakshmiB, MalhotraDet al. Strong association of de novo copy number mutations with autism. Science316(5823), 445–449 (2007).
  • Manning M , HudginsL; Professional Practice and Guidelines Committee. Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities. Genet. Med.12(11), 742–745 (2010).
  • Edelmann L , HirschhornK. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies. Ann. NY Acad. Sci.1151, 157–166 (2009).
  • Ylstra B , van den IjsselP, CarvalhoB, BrakenhoffRH, MeijerGA. BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH). Nucleic Acids Res.34(2), 445–450 (2006).
  • Kearney HM , SouthST, WolffDJ, LambA, HamoshA, RaoKW; Working Group of the American College of Medical Genetics. American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities. Genet. Med.13(7), 676–679 (2011).
  • Kearney HM , ThorlandEC, BrownKK, Quintero-RiveraF, SouthST; Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genet. Med.13(7), 680–685 (2011).

▪ Websites

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.