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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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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

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