Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria
Authors:
- 1 January 1987
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 110 (1) , 68-71
Abstract
No abstract availableKeywords
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- The Morbid Anatomy of the Human GenomeMedicine, 1986
- Gene Transfer and Expression of Human Phenylalanine HydroxylaseScience, 1985
- PRENATAL DIAGNOSIS OF CLASSIC PHENYLKETONURIA BY DNA ANALYSISThe Lancet, 1985
- Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in MediterraneansNature, 1984
- Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuriaNature, 1983
- Phenylketonuria: Epitome of Human Biochemical GeneticsNew England Journal of Medicine, 1980
- PHENYLKETONURIA AND OTHER PHENYLALANINE HYDROXYLATION MUTANTS IN MANAnnual Review of Genetics, 1980