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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...
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| Vydáno v: | Scientifica (Cairo) |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hindawi Publishing Corporation
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4804090/ https://ncbi.nlm.nih.gov/pubmed/27051557 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/5826431 |
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