Prenatal diagnosis of infantile GM 2 gangliosidosis type II...

Prenatal diagnosis of infantile GM 2 gangliosidosis type II (sandhoff disease) by detection of N-acetylglucosaminyl-oligosaccharides in amniotic fluid with high-performance liquid chromatography

Thomas G. Warner, M. Wilson Turner, Jennifer R. Toone, Derek Applegarth
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Volume:
6
Year:
1986
Language:
english
Pages:
8
DOI:
10.1002/pd.1970060602
File:
PDF, 403 KB
english, 1986
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