Inherited metabolic disorders in Turkey
- 5 October 1989
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (5) , 732-738
- https://doi.org/10.1007/bf01799576
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Consanguinity in Turkey in 1988.1989
- A simple concept for the screening of amino‐ and organic aciduriasJournal of Inherited Metabolic Disease, 1988
- Inborn Errors of Metabolism: The Clinical Diagnosis in Early InfancyPediatrics, 1987
- Screening for Metabolic Disease in a Metropolitan HospitalArchives of Pediatrics & Adolescent Medicine, 1982
- Screening for PhenylketonuriaPublished by Springer Nature ,1980
- Screening for organic acidurias and amino acidopathies in newborns and childrenJournal of Inherited Metabolic Disease, 1979
- Nonketotic HyperglycinemiaNew England Journal of Medicine, 1975
- SCREENING FOR BIOCHEMICAL ABNORMALITIES IN THE URINE OF THE MENTALLY HANDICAPPED IN DUBLINJournal of Intellectual Disability Research, 1972
- Improved method for measuring galactose-1-phosphate uridyl transferase activity of erythrocytesClinica Chimica Acta; International Journal of Clinical Chemistry, 1966
- Endemic Urinary Lithiasis in Turkish Children: A Clinical Study of 119 CasesArchives of Disease in Childhood, 1961