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PRJNA154859
SNP data from 30 pheochromocytomas and paragangliomas.
Source: NCBI BioProject (ID PRJNA154859)

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Project name: Homo sapiens
Description: SNP profiles from 30 pheochromocytomas and paragangliomas were analyzed to detect identical-by-descent haplotypes, highlighting a founder mutation of SDHD in two samples.Overall design: 30 pheochromocytomas and paragangliomas were analyzed with Illumina Human610-Quad v1.0 BeadChips.
Data type: Variation
Sample scope: Multiisolate
Relevance: Medical
Organization: Programme "Cartes d'Identité des Tumeurs", Ligue Contre Le Cancer
Literatures
  1. PMID: 22567117
Release date: 2012-03-23
Last updated: 2011-09-19