Genomics

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Affymetrix SNP array data for samples of 9 members of a FNMTC family


ABSTRACT: Familial nonmedullary thyroid cancer (FNMTC) is a disease with the inheritance pattern is autosomal dominant with incomplete penetrance, but the causative gene is not clear. To identify the disease related locus in the FNMTC family, whole-genome SNPs of nine family members (five affected and four unaffected) were genotyped. We analyzed the SNP data with a novel method and mapped the disease-causing gene to several regions on the whole genome.

ORGANISM(S): Homo sapiens

PROVIDER: GSE75312 | GEO | 2017/12/31

SECONDARY ACCESSION(S): PRJNA303172

REPOSITORIES: GEO

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