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hypoparathyroidism, autosomal dominant
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PTH
A reinvestigation of the amino-terminal sequence of human parathyroid hormone
A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism
Ectopic transcription of the parathyroid hormone gene in lymphocytes, lymphoblastoid cells and tumour tissue
Regional mapping of the parathyroid hormone gene (PTH) by cytogenetic and molecular studies
Structure-activity relation of NH2-terminal human parathyroid hormone fragments
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External
Studies of Inherited Diseases of Metabolism