SNP data from 30 pheochromocytomas and paragangliomas.
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE32204
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资源简介：
SNP profiles from 30 pheochromocytomas and paragangliomas were analyzed to detect identical-by-descent haplotypes, highlighting a founder mutation of SDHD in two samples. 30 pheochromocytomas and paragangliomas were analyzed with Illumina Human610-Quad v1.0 BeadChips.
创建时间：
2013-05-24
