(Q36586722)
Statements
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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 (English)
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H Bikker
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G J van Ommen
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J J de Vijlder
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1 January 1984
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67
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3
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301-305
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Identifiers
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