Literature DB >> 4191918

Prenatal diagnosis of type-II glycogenosis.

G Hug, W K Schubert, S Soukup.   

Abstract

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Year:  1970        PMID： 4191918     DOI： 10.1016/s0140-6736(70)91128-1

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's disease.

Authors:  A H Fensom; P F Benson; S Blunt; S P Brown; T M Coltart
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

Review 2.  Management of inherited metabolic disease.

Authors:  D N Raine
Journal:  Br Med J       Date:  1972-05-06

3.  Prenatal diagnosis and genetic counselling.

Authors:  D J Brock
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

Review 4.  The glycogen storage diseases.

Authors:  B E Ryman
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

5.  Antenatal diagnosis of mucopolysaccharidosis type I (Hurler's disease) is not possible by electron microscopy of uncultured amniotic fluid cells.

Authors:  G Hug; S Soukup; G Chuck; M Ryan
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318
  5 in total

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