SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome
The present study evaluated the role of SNP microarray in 101 cases of clinically suspected FISH negative (noninformative/normal) 22q11.2 microdeletion syndrome. SNP microarray was carried out using 300 K HumanCytoSNP-12 BeadChip array or CytoScan 750 K array. SNP microarray identified 8 cases of 22...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2016-01-01
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Series: | Scientifica |
Online Access: | http://dx.doi.org/10.1155/2016/5826431 |