SNP data from 30 pheochromocytomas and paragangliomas.

ABSTRACT: 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.

ORGANISM(S): Homo sapiens

SUBMITTER: Eric Letouzé 

PROVIDER: E-GEOD-32204 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress