Literature DB >> 8033936

Haplotype analysis and a new MspI-polymorphism at the phenylalanine hydroxylase gene in the Arabian population.

C Bender, A Büchler, B Schmidt-Mader, M Schlotter, A S Teebi, D S Konecki, F K Trefz.   

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Year:  1994        PMID： 8033936     DOI： 10.1007/bf01956432

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  5 in total

1.  Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.

Authors:  A S Lidsky; F D Ledley; A G DiLella; S C Kwok; S P Daiger; K J Robson; S L Woo
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

2.  Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.

Authors:  S C Kwok; F D Ledley; A G DiLella; K J Robson; S L Woo
Journal:  Biochemistry       Date:  1985-01-29       Impact factor: 3.162

3.  Phenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase gene.

Authors:  K J Hofman; G Steel; H H Kazazian; D Valle
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

4.  Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU).

Authors:  S P Daiger; R Chakraborty; L Reed; G Fekete; D Schuler; G Berenssi; I Nasz; R Brdicka; J Kamarýt; A Pijácková
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

5.  Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

Authors:  S P Daiger; L Reed; S S Huang; Y T Zeng; T Wang; W H Lo; Y Okano; Y Hase; Y Fukuda; T Oura
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025
  5 in total

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