See Also: hypoxanthine guanine phosphoribosyltransferase(medicine)
hypoxanthine guanine phosphoribosyltransferase deficiency(medicine)
hypoxanthine-guanine-xanthine phosphoribosyltransferase(medicine)
Masson's argentaffin stain(medicine)
hypoxanthine phosphoribosyltransferase(medicine)
hypoxanthine-guanine phosphoribosyl transferase(medicine)
hypoxanthine-guanine phosphoribosyl tranferase marker(medicine)
Masson's trichrome stain(medicine)
Fontana-Masson silver stain(medicine)
Masson-Fontana ammoniacal silver stain(medicine)
hypoxanthine guanine phosphoribosyltransferase deficiency (medicine) and Masson's argentaffin stain (medicine)
hypoxanthine guanine phosphoribosyltransferase deficiency (medicine)
hypoxanthine guanine phosphoribosyltransferase deficiency
A sex-linked inherited metabolic disorder; complete deficiency results in Lesch-Nyhan syndrome; incomplete deficiency is associated with acute gouty arthritis and renal stones.
Masson's argentaffin stain (medicine)
Masson's argentaffin stain
<technique> A stain used to stain enterochromaffin granules brown-black.
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