FIRST TRIMESTER DIAGNOSIS OF HUNTER SYNDROME ON CHORIONIC VILLI
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Efficient direct chromosome analysis and enzyme determinations from chorionic villi samples in the first trimester of pregnancy;Simoni;Hum Genet,1983
2. Prenatal diagnosis of sickle-cell anemia in the first trimester of pregnancy;Goossens;N Engl J Med,1983
3. Genetic metabolic diseases: Early diagnosis and prenatal analysis;Galjaard,1980
4. Feasibility of first-trimester prenatal diagnosis of Hunter syndrome;Lykkelund;Lancet,1983
5. Prenatal monitoring for the Hunter syndrome: The heterozygous female fetus;Kleijer;Clin Genet,1979
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1. First trimester chorionic villi sampling and direct chromosome preparations;Clinical Genetics;2008-04-23
2. Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay;Prenatal Diagnosis;2002
3. Recent advances in the prenatal diagnosis of the mucopolysaccharidoses;Prenatal Diagnosis;1994-01
4. Literaturverzeichnis;Manual der fetalen Medizin;1994
5. Degenerative cerebral diseases;Neurological Problems in Childhood;1993
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