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6. Inborn errors of metabolism. Variability within single diseases. Danks DM Clin Pediatr (Phila); 1971 Jan; 10(1):1-3. PubMed ID: 5545904 [No Abstract] [Full Text] [Related]
7. [Human genetics in hematological disorders]. Fujiki N; Shibuya Y; Saito T; Takebayashi M; Mibayashi E Saishin Igaku; 1967 Dec; 22(12):2676-85. PubMed ID: 4874574 [No Abstract] [Full Text] [Related]
8. The X chromosome and the eye. The implications of recent microbiological models for clinical ophthalmology. Warburg M Hum Hered; 1974; 24(5-6):389-414. PubMed ID: 4219211 [No Abstract] [Full Text] [Related]
10. Red cell enzymopathies as a model of inborn errors of metabolism. Miwa S; Kanno H; Hirono A; Fujii H Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088 [TBL] [Abstract][Full Text] [Related]
16. Pedigree of a family with hyper-alkaline-phosphatasemia apparently inherited as an autosomal recessive trait. Kawasaki S; Sano M; Nagumo F; Tadano J; Maeda T Clin Chim Acta; 1995 Jun; 238(1):109-11. PubMed ID: 7554291 [No Abstract] [Full Text] [Related]
17. [Enzyme defects as molecular diseases]. Aebi H Verh Dtsch Ges Inn Med; 1972; 78():304-13. PubMed ID: 4665667 [No Abstract] [Full Text] [Related]
18. Pharmacogenetics: defective enzymes in relation to reactions to drugs. La Du BN Annu Rev Med; 1972; 23():453-68. PubMed ID: 4118885 [No Abstract] [Full Text] [Related]
19. Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family. Frydman M; Straussberg R; Shomrat R; Goebel H; Legum C; Shiloh Y Am J Med Genet; 1995 Sep; 58(3):209-12. PubMed ID: 8533818 [TBL] [Abstract][Full Text] [Related]