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Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

Restriction Site PolymorphismUnusual ScarcityAllelic VariantAllergyGenetic DisorderGeneticsMolecular GeneticsGenetic VariationMedicineHeritabilityGenetic BasisHuman Thyroglobulin Gene