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9. Variation in argininosuccinate synthetase activity in amniotic fluid cell cultures: implications for prenatal diagnosis of citrullinemia. Jacoby LB; Shih VE; Struckmeyer C; Niermeijer MF; Boué J Clin Chim Acta; 1981 Oct; 116(1):1-7. PubMed ID: 7318168 [TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of citrullinaemia: review of a 10-year experience including recent use of DNA analysis. Northrup H; Beaudet AL; O'Brien WE Prenat Diagn; 1990 Dec; 10(12):771-9. PubMed ID: 2075179 [TBL] [Abstract][Full Text] [Related]
11. Improved standards for prenatal diagnosis of citrullinemia. Miller MJ; Soler-Alfonso CR; Grund JE; Fang P; Sun Q; Elsea SH; Sutton VR Mol Genet Metab; 2014 Jul; 112(3):205-9. PubMed ID: 24889030 [TBL] [Abstract][Full Text] [Related]
12. Prenatal exclusion of the HHH syndrome. Gray RG; Green A; Hall S; McKeown C Prenat Diagn; 1995 May; 15(5):474-6. PubMed ID: 7644438 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of bovine citrullinaemia. Healy P; Dennis J; Rawlinson R; Andersson L Res Vet Sci; 1993 Nov; 55(3):271-4. PubMed ID: 8284487 [TBL] [Abstract][Full Text] [Related]
15. Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villi. Christensen E; Brandt NJ; Philip J; Bang J Prenat Diagn; 1985; 5(4):299-301. PubMed ID: 4048069 [TBL] [Abstract][Full Text] [Related]
16. The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency. Robinson BH; Oei J; Sherwood WG; Applegarth D; Wong L; Haworth J; Goodyer P; Casey R; Zaleski LA Am J Hum Genet; 1984 Mar; 36(2):283-94. PubMed ID: 6424438 [TBL] [Abstract][Full Text] [Related]
17. Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy. Suormala T; Fowler B; Jakobs C; Duran M; Lehnert W; Raab K; Wick H; Baumgartner ER Eur J Pediatr; 1998 Jul; 157(7):570-5. PubMed ID: 9686819 [TBL] [Abstract][Full Text] [Related]
18. [Attempt at antenatal diagnosis of argininosuccinic aciduria]. Dhondt JL; Farriaux JP; Pollitt RJ; Vamos E; Richard P; Blanckaert D; Delecour M; Monnier JC; Fontaine G Ann Genet; 1976 Mar; 19(1):23-7. PubMed ID: 1084118 [TBL] [Abstract][Full Text] [Related]
19. Pitfalls in the prenatal diagnosis of propionic acidemia. Buchanan PD; Kahler SG; Sweetman L; Nyhan WL Clin Genet; 1980 Sep; 18(3):177-83. PubMed ID: 6934053 [TBL] [Abstract][Full Text] [Related]
20. Detection of kinetically abnormal argininosuccinate synthase in neonatal citrullinemia by conversion of citrulline to arginine in intact fibroblasts. Ben-Yoseph Y; Mitchell DA Clin Chim Acta; 1989 Aug; 183(2):125-33. PubMed ID: 2791302 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]