Identification ofheterozygous genotype for cystinosis in utero by a new pulse-labeling technique: Preliminary report
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference9 articles.
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2. Biochemical diagnosis of an X-linked disease in utero;Fujimoto;Lancet,1968
3. Prenatal detection of genetic defects;Nadler;J. Pediat.,1969
4. Lesch-Nyhan mutation: Prenatal detection with amniotic fluid cells;DeMars;Science,1969
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1. Gene dosage and antigenic expression on the cell surface of bovine erythrocytes1;Animal Blood Groups and Biochemical Genetics;2009-04-24
2. Renal Tubular Disorders in the Neonate;Clinics in Perinatology;1992-03
3. A high performance liquid chromatography method for the analysis of 35S-cystine: Application to the diagnosis of cystinosis;Clinica Chimica Acta;1989-09
4. Cystinosis Coming of Age;Advances in Pediatrics;1986
5. Prenatal Diagnosis of Miscellaneous Biochemical Disorders;Genetic Disorders and the Fetus;1986
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