Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Hereditary non-medullary thyroid cancer 3 is an autosomal dominant disorder caused by mutations in the chromosomal region 2q21.
| 1. |
Burgess JR et al. (1997) Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid. 
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| 2. |
Vriens MR et al. (2009) Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer.
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| 3. |
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.
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| 4. |
McKay JD et al. (2001) Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.
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| 5. |
OMIM.ORG article Omim 606240
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