Author:
Lissens W.,Van Lierde M.,Decaluwe J.,Foulon W.,Evrard P.,van Hoof F.,Freund M.,Liebaers I.
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference5 articles.
1. , , , (1978). Enzymic diagnosis of the genetic mucopolysaccharide storage disorders. In: (Ed.). Methods in Enzymology, Vol. 50, New York: Academic Press, 439–456.
2. Sequential thin layer chromatography of urinary acidic glycosaminglycans
3. Iduronate sulfatase in amniotic fluid: An aid in the prenatal diagnosis of the Hunter syndrome
4. , (1983). The mucopolysaccharide storage diseases. In: , , , (Eds). The Metabolic Basis of Inherited Disease, 5th ed., New York: McGraw-Hill, 751–777.
5. Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans
Cited by
8 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献