Osteodysmetamorphosis Foetalis a Newly Discovered Characteristic Skeletal Disease Showing Low Serum and Tissue Alkaline Phosphatase Activity (Hypophosphatasia)
- 1 January 1956
- book chapter
- Published by Wiley
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Osteodysmetamorphosis fetalis: A clinical-pathological study of a congenital skeletal disease withretarded growth, hypophosphatasemia and renal damageThe Journal of Pediatrics, 1954
- "HYPOPHOSPHATASIA"American Journal of Diseases of Children, 1948
- An improved King and Armstrong method for the determination of phosphatase activity in blood serum.Acta Medica Scandinavica, 1939