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32. [SYNDROME OF DEFECTIVE INTESTINAL ABSORPTION IN THE CHILD. (CELIAC SYNDROME)]. MUNOZTURNBULL J Rev Colomb Pediatr Pueric; 1963 Jun; 21():133-48. PubMed ID: 14125658 [No Abstract] [Full Text] [Related]
33. [Variations in the expression of the pyruvate kinase deficiency of erythrocytes]. Bentegeat J; Verger P; de Joigny C; Boisseau M; Roulaud F Nouv Rev Fr Hematol; 1968; 8(6):856-63. PubMed ID: 4236869 [No Abstract] [Full Text] [Related]
34. [HEREDITARY DISEASES DUE TO METABOLISM DISORDERS]. BOUHAHA M Tunis Med; 1964; 42():363-77. PubMed ID: 14274009 [No Abstract] [Full Text] [Related]
35. A CLINICIAN'S VIEW OF GENETICS IN MEDICINE. PLOTZ EJ N Y State J Med; 1965 Jun; 65():1628-34. PubMed ID: 14302195 [No Abstract] [Full Text] [Related]
36. OXIDATIVE HEMOLYSIS AND ERYTHROCYTE METABOLISM IN HEREDITARY ACATALASIA. JACOB HS; INGBAR SH; JANDL JH J Clin Invest; 1965 Jul; 44(7):1187-99. PubMed ID: 14328395 [No Abstract] [Full Text] [Related]
37. [Pathogenesis of acanthocytosis]. REY J; FREZAL J; LAMY M Nouv Rev Fr Hematol; 1963; 3():60-2. PubMed ID: 13981884 [No Abstract] [Full Text] [Related]