FAMILIAL FANCONI SYNDROME WITH MALABSORPTION AND GALACTOSE INTOLERANCE, NORMAL KINASE AND TRANSFERASE ACTIVITY.
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1981.tb05735.x/fullpdf
Reference20 articles.
1. TEST-MEAL IN THE DIAGNOSIS OF MALABSORPTION IN INFANCY.
2. 2. H. Behrendt, Diagnostic tests for infants and children . 1st ed . Philadelphia: Lea & Febiger, 1949 : 115 -20 .
3. A PATIENT WITH HEREDITARY GALACTOKINASE DEFICIENCY
4. RENAL FUNCTIONAL CHANGES IN ACUTE GLOMERULONEPHRITIS IN CHILDREN. A ONE-YEAR FOLLOW-UP
5. ANO-RECTAL MANOMETRY IN THE DIAGNOSIS OF HIRSCHSPRUNG'S DISEASE IN INFANTS
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