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Prenatal-diagnosis of Hunter Syndrome Using Fetal Plasma

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Lissens, W. Vanlierde, M. Decaluwe, J. Foulon, W. Evrard, Philippe [UCL] Liebaers, I.
Document type Article de périodique (Journal article) – Article de recherche
Publication date 1988
Language Anglais
Journal information "Prenatal Diagnosis" - Vol. 8, no. 1, p. 59-62 (1988)
Peer reviewed yes
Publisher John Wiley & Sons Ltd (W Sussex)
issn 0197-3851
e-issn 1097-0223
Publication status Publié
Affiliation UCL
Links
  1. , , , (1978). Enzymic diagnosis of the genetic mucopolysaccharide storage disorders. In: (Ed.). Methods in Enzymology, Vol. 50, New York: Academic Press, 439–456.
  2. Humbel, Clin. Chim. Acta, 50, 290 (1972)
  3. Liebaers, J Pediatr., 90, 423 (1977)
  4. , (1983). The mucopolysaccharide storage diseases. In: , , , (Eds). The Metabolic Basis of Inherited Disease, 5th ed., New York: McGraw-Hill, 751–777.
  5. Mossman, Prenat. Diagn., 2, 169 (1982)
Bibliographic reference Lissens, W. ; Vanlierde, M. ; Decaluwe, J. ; Foulon, W. ; Evrard, Philippe ; et. al. Prenatal-diagnosis of Hunter Syndrome Using Fetal Plasma. In: Prenatal Diagnosis, Vol. 8, no. 1, p. 59-62 (1988)
Permanent URL http://hdl.handle.net/2078.1/53301