Literature DB >> 5811698

The newborn phenylketonuria screening program in Ontario.

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Year:  1969        PMID： 5811698      PMCID： PMC1946107     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN： 0008-4409            Impact factor:   8.262


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  6 in total

1.  CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA.

Authors:  M W PARTINGTON; R M ANDERSON
Journal:  Can Med Assoc J       Date:  1964-06-06       Impact factor: 8.262

Review 2.  PHENYLKETONURIA. A REVIEW OF SOME DEFICITS IN OUR INFORMATION.

Authors:  D S KLEINMAN
Journal:  Pediatrics       Date:  1964-01       Impact factor: 7.124

3.  Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuria.

Authors:  V H AUERBACH; A M DIGEORGE; M P BRIGHAM; J M DOBBS
Journal:  J Pediatr       Date:  1963-06       Impact factor: 4.406

4.  Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood.

Authors:  M W Partington
Journal:  Can Med Assoc J       Date:  1968-10-05       Impact factor: 8.262

5.  Transient tyrosinemia of the newborn: dietary and clinical aspects.

Authors:  M E Avery; C L Clow; J H Menkes; A Ramos; C R Scriver; L Stern; B P Wasserman
Journal:  Pediatrics       Date:  1967-03       Impact factor: 7.124

6.  Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria.

Authors:  A J Schneider; S D Garrard
Journal:  J Pediatr       Date:  1966-05       Impact factor: 4.406
  6 in total
  1 in total

1.  Ethnic variation in genetic disease: possible roles of hitchhiking and epistasis.

Authors:  D K Wagener; L L Cavalli-Sforza
Journal:  Am J Hum Genet       Date:  1975-05       Impact factor: 11.025
  1 in total

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