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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Detalles Bibliográficos
Autores principales: Halder, Ashutosh, Jain, Manish, Kalsi, Amanpreet Kaur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804090/
https://www.ncbi.nlm.nih.gov/pubmed/27051557
http://dx.doi.org/10.1155/2016/5826431

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804090/
https://www.ncbi.nlm.nih.gov/pubmed/27051557
http://dx.doi.org/10.1155/2016/5826431

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