Non-medullary thyroid cancer 3
Hereditary non-medullary thyroid cancer 3 is an autosomal dominant disorder caused by mutations in the chromosomal region 2q21.
Burgess JR et al. (1997) Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid.[^]
Vriens MR et al. (2009) Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer.[^]
McKay JD et al. (1999) At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family.[^]
McKay JD et al. (2001) Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.[^]
OMIM.ORG articleOmim 606240 [^]