(Q51861706)
Statements
The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern. (English)
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K R van der Ploeg
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B G Wolthers
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G T Nagel
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M Volmer
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N M Drayer
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1 April 1982
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120
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3
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341-353
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