Literature DB >> 13702464

A case of phenylketonuria in the Eta resulting from the mating of a homozygous father and a heterozygous mother.

N FUJIKI, A L DREW, M MIYAKE, H NEMOTO, C SUJAKU, T SHIMADA.   

Abstract

Entities:  

Keywords:  CONSANGUINITY; PHENYLPYRUVIC OLIGOPHRENIA/genetics

Mesh：

Year:  1961        PMID： 13702464      PMCID： PMC1932102     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  4 in total

1.  [A colorimetric method for the quantitative determination of phenyl pyruvic acid in urine].

Authors:  K KROPP; K LANG
Journal:  Klin Wochenschr       Date:  1955-05-15

2.  Method for determination of serum phenylalanine with use of the Kapeller-Adler reaction.

Authors:  R J HENRY; C SOBEL; N CHIAMORI
Journal:  AMA J Dis Child       Date:  1957-12

3.  Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria.

Authors:  K W DRISCOLL; D Y HSIA; W E KNOX; W TROLL
Journal:  Nature       Date:  1956-12-01       Impact factor: 49.962

4.  Metabolic studies in phenylketonuria.

Authors:  L Penrose; J H Quastel
Journal:  Biochem J       Date:  1937-02       Impact factor: 3.857
  4 in total
  1 in total

1.  Variations in intelligence in phenylktonuria.

Authors:  M W PARTINGTON
Journal:  Can Med Assoc J       Date:  1962-04-21       Impact factor: 8.262
  1 in total

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