Mucopolysaccharidosis type VII associated with hydrops fetalis: histopathological and ultrastructural features with genetic implications.

Author:

Molyneux A J,Blair E,Coleman N,Daish P

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference10 articles.

1. Hydrops fetalis and other forms of excess fluid accumulation in the fetus;Keeling, J.W.,1991

2. Inborn metabolic diseases of the perinatal infant;Dimmick, J.E.; Applegarth, D.A.,1991

3. The metabolic and molecular basis of inherited disease;Neufeld, E.F.,1995

4. Cloning and characterisation of the human beta-glucuronidase gene;true;Genomics,1990

5. Four novel mutations in mucopolysaccharidosis type VII including a unique base substitution in exon 10 of the beta-glucuronidase gene that creates a novel 5' splice site;Yamada, S.; Tomatsu, S.; Sly, W.S.; Islam, R.; Wenger, D.A.; Fukuda, S.;Hum Mol Genet,1994

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