Literature DB >> 19975693

Healed Double Empyema.

E M Corner, L Grant.   

Abstract

Entities:  

Year:  1912        PMID： 19975693      PMCID： PMC2006083     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  3 in total

1.  Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study.

Authors:  P Guldberg; H L Levy; W B Hanley; R Koch; R Matalon; B M Rouse; F Trefz; F de la Cruz; K F Henriksen; F Güttler
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

2.  Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.

Authors:  P Guldberg; H L Levy; K F Henriksen; F Guttler
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

3.  Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland.

Authors:  P Guldberg; K F Henriksen; I Sipilä; F Güttler; A de la Chapelle
Journal:  J Med Genet       Date:  1995-12       Impact factor: 6.318
  3 in total

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