Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Congenital nongoitrous hypothyroidism 3 is a disorder whose genetic background is not yet fully understood.
| 1. |
Mimouni M et al. (1996) Familial hypothyroidism with autosomal dominant inheritance. 
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| 2. |
Grasberger H et al. (2005) Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate loci.
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| 3. |
Grasberger H et al. (2005) Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1.
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| 4. |
OMIM.ORG article Omim 609893
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