Literature DB >> 4409025

[Congenital adrenogenital syndrome with unusually light 21-hydroxylase deficiency].

W Andler, P Malvaux, M Zachmann, A Prader.   

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Year:  1974        PMID： 4409025

Source DB:  PubMed          Journal:  Monatsschr Kinderheilkd


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  1 in total

1.  Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.

Authors:  J Homoki; J Solyom; W M Teller
Journal:  Eur J Pediatr       Date:  1988-04       Impact factor: 3.183
  1 in total

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