Prenatal diagnosis of cystic fibrosis by trehalase enzyme assay in amniotic fluid
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb01211.x/fullpdf
Reference14 articles.
1. Peptidases in amniotic fluid: low values in cystic fibrosis;Baker;Lancet,1983
2. Amniotic fluid alkaline phosphatase isoenzymes in early prenatal diagnosis of cystic fibrosis;Brock;Lancet,1983
3. Microvillar peptidase activity in amniotic fluid: possible use in the prenatal diagnosis of cystic fibrosis;Carbarns;Lancet,1983
4. Method for assay of intestinal disaccharidases;Dahlqvist;Anal. Biochem.,1964
5. Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses;Morin;Clin. Genet.,1980
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1. Amniotic fluid microvillar enzyme activity in fetal malformations;Clinical Genetics;2008-06-28
2. An abnormal pattern of amniotic fluid microvillar enzymes signalling fetal cystic fibrosis;Clinical Genetics;2008-06-28
3. Intestinal Brush Border Glycohydrolases: Structure, Function, and Development;Critical Reviews in Biochemistry and Molecular Biology;1995-01
4. Discriminant analysis for assessing the value of amniotic fluid microvillar enzymes in the prenatal diagnosis of cystic fibrosis;Prenatal Diagnosis;1990-12
5. Erfahrungen mit der pränatalen Diagnostik in Ungarn;Pränatale Diagnostik;1989
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