Author:
G�ttler F.,DiLella A. G.,Ledley F. D.,Lidsky A. S.,Kvok S. C. M.,Marvit J.,Woo S. L. C.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference19 articles.
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2. Daiger S, Lidsky AS, Chakraborty R, Koch R, Güttler F, Woo SLC (1986) Effective use of polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria. Lancet I:229?232
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4. DiLella AG, Marvit J, Lidsky AS, Güttler F, Woo SLC (1986) Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria. Nature 322:799?803
5. Güttler F (1980) Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood. Acta Pediatr Scand [Suppl] 280:1?80
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