Yüklüyor......
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...
Kaydedildi:
| Yayımlandı: | Scientifica (Cairo) |
|---|---|
| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Hindawi Publishing Corporation
2016
|
| Konular: | |
| Online Erişim: | 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 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|