(Q42476757)
Statements
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A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases (English)
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Yano K
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Hidaka A
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Saji M
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Polymeropoulos MH
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Okuno A
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Kohn LD
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Cutler GB Jr
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1 December 1994
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79
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6
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1818-1823
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Identifiers
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