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2. [The chromosome mapping of enzymatic genes related to inborn metabolic errors]. Yoshida MC Nihon Rinsho; 1995 May; 53(5):1075-80. PubMed ID: 7602758 [TBL] [Abstract][Full Text] [Related]
3. [Hemolytic anemias due to enzymopathies]. Rosa R Rev Prat; 1993 Jun; 43(11):1397-402. PubMed ID: 8235390 [TBL] [Abstract][Full Text] [Related]
4. Red cell enzyme deficiencies: from genetic basis to gene transfer. Mason PJ Semin Hematol; 1998 Apr; 35(2):126-35. PubMed ID: 9565155 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Inborn errors of metabolism--a review of some general concepts. Danks DM Aust N Z J Med; 1981 Jun; 11(3):309-20. PubMed ID: 7028024 [No Abstract] [Full Text] [Related]
7. [Current achievements, problems and prospects in the study of hereditary enzymopathies in humans]. Vidershaĭn GIa Vestn Akad Med Nauk SSSR; 1986; (10):81-8. PubMed ID: 3541441 [No Abstract] [Full Text] [Related]
8. Metabolic consequences of genetic defects in lysosomes. Tager JM; Jonsson LV; Aerts JM; Elferink RP; Schram AW; Erickson AH; Barranger JA Biochem Soc Trans; 1984 Dec; 12(6):902-5. PubMed ID: 6530036 [No Abstract] [Full Text] [Related]
9. Nonketotic hyperglycinemia in a patient with the 9p- syndrome. Burton BK; Pettenati MJ; Block SM; Bensen J; Roach ES Am J Med Genet; 1989 Apr; 32(4):504-5. PubMed ID: 2773994 [TBL] [Abstract][Full Text] [Related]
10. Differential diagnosis and diseases due to enzyme changes. Martin-DeLeon PA Del Med J; 1979 May; 51(5):267-70, 276-81. PubMed ID: 110628 [No Abstract] [Full Text] [Related]
12. [Metabolic myopathies]. Finocchiaro G; Zeviani M; Garavaglia B; Gellera C; Bertagnolio B; Rimoldi M; Di Donato S Minerva Pediatr; 1991 Mar; 43(3):81-9. PubMed ID: 1870530 [No Abstract] [Full Text] [Related]
13. [Chromosome mapping of metabolic disorder]. Yoshida MC Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):457-60. PubMed ID: 3270850 [No Abstract] [Full Text] [Related]
14. [Hereditary enzymopathies: problems and prospects]. Vidershoĭn GIa Vopr Med Khim; 1982; 28(3):22-31. PubMed ID: 7048733 [No Abstract] [Full Text] [Related]
15. [Separate nosologic entity of the 18q syndrome. Localization of the peptidase A gene in man]. Manikowska E; Lambert I; Jankowska B; Czerski P; Pieta H; Kurniewicz-Witczak R; Langner B Pediatr Pol; 1978 Oct; 53(10):1159-67. PubMed ID: 714544 [No Abstract] [Full Text] [Related]
16. [Prenatal diagnosis of inborn errors of metabolism. 155 cases (author's transl)]. Boué J; Nicolas H; Cheruy C; Couillin P; Boué A Nouv Presse Med; 1982 Mar; 11(13):979-83. PubMed ID: 7070985 [TBL] [Abstract][Full Text] [Related]
17. [Genetic mapping of chromosome X: known localizations]. Verellen-Dumoulin C J Genet Hum; 1989 Dec; 37(4-5):321-51. PubMed ID: 2699742 [TBL] [Abstract][Full Text] [Related]
18. A new look at the inborn errors of metabolism. Sinclair L Ann Clin Biochem; 1982 Jul; 19 (Pt 4)():314-21. PubMed ID: 6812485 [No Abstract] [Full Text] [Related]