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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990
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developmental retardation
dysmorphic
genetic linkage
hepatosplenomegaly
Hunter's syndrome
hypotonia
hypotonia,infants
macrocephaly
mucopolysaccharidoses
mucopolysacchariduria
RFLPs

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