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Genet Med. 2010 Nov;12(11):742-5. doi: 10.1097/GIM.0b013e3181f8baad.

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

Author information

1
Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA. mmanning@stanford.edu

Abstract

Laboratory evaluation of patients with developmental delay/intellectual disability, congenital anomalies, and dysmorphic features has changed significantly in the last several years with the introduction of microarray technologies. Using these techniques, a patient's genome can be examined for gains or losses of genetic material too small to be detected by standard G-banded chromosome studies. This increased resolution of microarray technology over conventional cytogenetic analysis allows for identification of chromosomal imbalances with greater precision, accuracy, and technical sensitivity. A variety of array-based platforms are now available for use in clinical practice, and utilization strategies are evolving. Thus, a review of the utility and limitations of these techniques and recommendations regarding present and future application in the clinical setting are presented in this study.

PMID:
20962661
PMCID:
PMC3111046
DOI:
10.1097/GIM.0b013e3181f8baad
[Indexed for MEDLINE]
Free PMC Article

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