Gm1-gangliosidosis type I: In utero detection and fetal manifestations
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference16 articles.
1. Familial neurovisceral lipidosis;Landing;Am. J. Dis. Child.,1964
2. Generalized gangliosidosis;O'Brien;J. Pediatr.,1969
3. Generalized gangliosidosis: Beta-galactosidase deficiency;Okada;Science,1968
4. Leukocyte beta-galactosidase activity in the diagnosis of generalized Gm1-gangliosidosis;Singer;Pediatrics,1972
5. Intrauterine diagnosis: Comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cells;Kaback;Pediatr. Res.,1971
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3. Lysosomal enzyme levels in human amniotic fluid cells in tissue culture: III, β-glucuronidase, N-acetyl-β-D-glucosaminidase, α-mannosidase and acid phosphatase;Clinical Genetics;2008-04-23
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5. A case of GM1gangliosidosis type I;Ophthalmic Paediatrics and Genetics;1989-01
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