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6. Application of a galactosylceramidase microassay method to early prenatal diagnosis of Krabbe's disease. Tsutsumi O, Satoh K, Sakamoto S, Suzuki Y, Kato T. Clin Chim Acta; 1982 Nov 10; 125(3):265-73. PubMed ID: 7172437 [Abstract] [Full Text] [Related]
16. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis]. Dreyfus JC, Poenaru L. Ann Biol Clin (Paris); 1975 May 21; 33(6):465-72. PubMed ID: 818927 [Abstract] [Full Text] [Related]
17. Use of microtechniques for the detection of lysosomal enzyme disorders: Tay-Sachs disease, Gm1-gangliosidosis and Fabry disease. Bladon MT, Milunsky A. Clin Genet; 1978 Dec 21; 14(6):359-66. PubMed ID: 215359 [Abstract] [Full Text] [Related]
18. Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II). Aula P, Rapola J, Autio S, Raivio K, Karjalainen O. J Pediatr; 1975 Aug 21; 87(2):221-6. PubMed ID: 168339 [Abstract] [Full Text] [Related]
20. Prenatal exclusion of metachromatic leukodystrophy by estimation of arylsulphatase A activity in chorion and cultured amniotic fluid cells. Tsvetkova IV, Zolotukhina TV, Bakharev VA, Rosenfeld EL, Rosovsky IS. Prenat Diagn; 1983 Jul 21; 3(3):233-6. PubMed ID: 6137815 [Abstract] [Full Text] [Related] Page: [Next] [New Search]