(Q50567202)
Statements
Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism associated with mutations in the human Ca2+-sensing receptor gene in three Danish families. (English)
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Larsen NE
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Lønborg Friis IM
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Lillquist K
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Brown EM
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Gammeltoft S
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1 May 2000
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60
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3
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221-227
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