Literature DB >> 6472974

Prenatal diagnosis and carrier detection of classic phenylketonuria by gene analysis.

S L Woo.   

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Year:  1984        PMID： 6472974

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  4 in total

Review 1.  Phenylketonuria: old disease, new approach to treatment.

Authors:  H L Levy
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

2.  A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia.

Authors:  Y Okano; R C Eisensmith; M Dasovich; T Wang; F Güttler; S L Woo
Journal:  Eur J Pediatr       Date:  1991-03       Impact factor: 3.183

3.  The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.

Authors:  C B Newgard; R J Fletterick; L A Anderson; R V Lebo
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025

4.  Phenylketonuria: distribution of DNA diagnostic patterns in German families.

Authors:  C Aulehla-Scholz; M Vorgerd; E Sautter; D Leupold; R Mahlmann; K Ullrich; K Olek; J Horst
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132
  4 in total

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