Literature DB >> 13492000

Penylketonuria detection of the heterozygous carrier.

D Y Y HSIA, R S PAINE.   

Abstract

Keywords:  PHENYLPYRUVIC OLIGOPHRENIA/heredity

Mesh：

Year:  1957        PMID： 13492000

Source DB:  PubMed          Journal:  J Ment Defic Res        ISSN： 0022-264X


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  4 in total

1.  Recent work on phenylketonuria and maple syrup urine disease (leucinosis).

Authors:  L I WOOLF
Journal:  Proc R Soc Med       Date:  1962-10

2.  Phenylalanine metabolism and folic acid antagonists.

Authors:  T L GOODFRIEND; S KAUFMAN
Journal:  J Clin Invest       Date:  1961-09       Impact factor: 14.808

3.  Developmental Trajectories of Executive and Verbal Processes in Children with Phenylketonuria.

Authors:  Zoë W Hawks; Michael J Strube; Neco X Johnson; Dorothy K Grange; Desirée A White
Journal:  Dev Neuropsychol       Date:  2018-02-12       Impact factor: 2.253

4.  Detection of phenylketonuria carriers.

Authors:  S Kelly; F Rose
Journal:  Public Health Rep       Date:  1969-02       Impact factor: 2.792
  4 in total

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