Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference13 articles.
1. ANTENATAL DETECTION OF HURLER'S SYNDROME
2. Early Prenatal Diagnosis of Hurler's Syndrome with Termination of Pregnancy and Confirmatory Findings on the Fetus
3. ANTENATAL DIAGNOSIS OF MUCOPOLYSACCHARIDOSES
4. The measurement of acid mucopolysaccharides (glycosaminoglycans) in amniotic fluid and urine
5. , , (1977). Microtechniques in prenatal diagnosis of genetic disease. In: (Eds). Proceedings of the 5th International Congress on Human Genetics, Amsterdam: Excerpta Medica, 194–206.
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1. Mass spectrometry and two-dimensional electrophoresis in prenatal diagnosis of mucopolysaccharidosis type VI;Egyptian Journal of Medical Human Genetics;2022-02-11
2. Prenatal diagnosis of mucopolysaccharidoses type II by two‐dimensional electrophoresis and mass spectrometry in amniotic fluid;Journal of Obstetrics and Gynaecology Research;2022-01-13
3. Mucopolysaccharidoses diagnosis in the era of enzyme replacement therapy in Egypt;Heliyon;2021-08
4. Newborn screening for mucopolysaccharidoses: Measurement of glycosaminoglycans by LC-MS/MS;Molecular Genetics and Metabolism Reports;2020-03
5. Mucopolysaccharidosis 4;Atlas of Genetic Diagnosis and Counseling;2017
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