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3. [Present-day concepts on inborn errors of metabolism]. Frézal J; Rey J; Rey F Acta Univ Carol Med Monogr; 1973; 56():151-7. PubMed ID: 4524751 [No Abstract] [Full Text] [Related]
4. Common and rare alleles. Harris H Sci Prog; 1974; 61(244):495-514. PubMed ID: 4610744 [No Abstract] [Full Text] [Related]
5. [Hereditary enzymopathies: problems and prospects]. Vidershoĭn GIa Vopr Med Khim; 1982; 28(3):22-31. PubMed ID: 7048733 [No Abstract] [Full Text] [Related]
6. The detection of heterozygous carriers. Hsia DY Med Clin North Am; 1969 Jul; 53(4):857-74. PubMed ID: 4892641 [No Abstract] [Full Text] [Related]
7. Estimation of the frequency of the recessive gene of acatalasemia in Japan. Ogata M; Hayashi S; Takahara S Acta Med Okayama (1952); 1971 Jun; 25(3):193-8. PubMed ID: 4263520 [No Abstract] [Full Text] [Related]
9. Metabolic interference and the + - heterozygote. a hypothetical form of simple inheritance which is neither dominant nor recessive. Johnson WG Am J Hum Genet; 1980 May; 32(3):374-86. PubMed ID: 6770678 [TBL] [Abstract][Full Text] [Related]
10. Deficiency of alpha-antitrypsin in childhood liver disease. Johnson AM; Alper CA Pediatrics; 1970 Dec; 46(6):921-5. PubMed ID: 5491445 [No Abstract] [Full Text] [Related]
11. Uridine diphosphate galactose 4-epimerase deficiency. II. Clinical follow-up, biochemical studies and family investigation. Gitzelmann R; Steinmann B Helv Paediatr Acta; 1973 Dec; 28(6):497-510. PubMed ID: 4785150 [No Abstract] [Full Text] [Related]
12. An evolutionary advantage of haploidy in large yeast populations. Zeyl C; Vanderford T; Carter M Science; 2003 Jan; 299(5606):555-8. PubMed ID: 12543972 [TBL] [Abstract][Full Text] [Related]
13. Biochemical foundations of preventive medicine: the study of abnormal enzymes. Zakim D Horiz Biochem Biophys; 1974; 1():97-137. PubMed ID: 4219778 [No Abstract] [Full Text] [Related]
14. Induction of galactokinase in fibroblasts from heterozygous and homozygous subjects. Zacchello F; Benson PF; Brown S; Croll P; Giannelli F Nat New Biol; 1972 Sep; 239(90):95-6. PubMed ID: 4512833 [No Abstract] [Full Text] [Related]
15. [Genetic errors of glycoprotein metabolism]. Durand P Pediatr Med Chir; 1982; 4(3):177-84. PubMed ID: 7170188 [TBL] [Abstract][Full Text] [Related]
17. Variation in protein structure and inborn errors in metabolism. Poole AE Dent Clin North Am; 1975 Jan; 19(1):47-62. PubMed ID: 803265 [No Abstract] [Full Text] [Related]
18. Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS). Miller M; Brooks J; Forbes N; Insel R Prog Clin Biol Res; 1992; 375():495-8. PubMed ID: 1438393 [No Abstract] [Full Text] [Related]