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12. First-trimester prenatal diagnosis of tyrosinemia type I by amniotic fluid succinylacetone determination. Jakobs C; Stellaard F; Kvittingen EA; Henderson M; Lilford R Prenat Diagn; 1990 Feb; 10(2):133-4. PubMed ID: 2343022 [No Abstract] [Full Text] [Related]
13. Non-ketotic hyperglycinaemia: glycine/serine ratio in amniotic fluid--an unreliable method for prenatal diagnosis. Garcia-Muñoz MJ; Belloque J; Merinero B; Pérez-Cerdá C; Sanz P; Ugarte M Prenat Diagn; 1989 Jul; 9(7):473-6. PubMed ID: 2505247 [TBL] [Abstract][Full Text] [Related]
14. Early prenatal diagnosis of hereditary tyrosinaemia. Pettit BR; Kvittingen EA; Leonard JV Lancet; 1985 May; 1(8436):1038. PubMed ID: 2859481 [No Abstract] [Full Text] [Related]
15. Prenatal detection of defects in propionate metabolism. Wendel U Clin Chim Acta; 1980 Dec; 108(3):475-7. PubMed ID: 7471478 [No Abstract] [Full Text] [Related]
16. Glycine/serine ratios in amniotic fluid: an unreliable indicator for the prenatal diagnosis of nonketotic hyperglycinemia. Mesavage C; Nance CS; Flannery DB; Weiner DL; Suchy SF; Wolf B Clin Genet; 1983 May; 23(5):354-8. PubMed ID: 6406113 [No Abstract] [Full Text] [Related]
17. Prenatal diagnosis and family studies in a case of propionicacidaemia. Gompertz D; Goodey PA; Thom H; Russell G; Johnston AW; Mellor DH; MacLean MW; Ferguson-Smith ME; Ferguson-Smith MA Clin Genet; 1975 Oct; 8(4):244-50. PubMed ID: 1183068 [TBL] [Abstract][Full Text] [Related]
19. The antenatal diagnosis and aid to the management of hereditary tyrosinaemia by use of a specific and sensitive GC-MS assay for succinylacetone. Pettit BR; MacKenzie F; King GS; Leonard JV J Inherit Metab Dis; 1984; 7 Suppl 2():135-6. PubMed ID: 6434868 [No Abstract] [Full Text] [Related]
20. Prenatal diagnosis of non-ketotic hyperglycinaemia: experience in 50 at-risk pregnancies. Toone JR; Applegarth DA; Levy HL J Inherit Metab Dis; 1994; 17(3):342-4. PubMed ID: 7807948 [No Abstract] [Full Text] [Related] [Next] [New Search]