Literature DB >> 7054742

American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism.

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Year:  1982        PMID： 7054742

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


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  5 in total

1.  A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerations.

Authors:  I B Sardharwalla; J E Wraith
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

2.  Finnish national screening for hypothyroidism. Few false positives, early therapy.

Authors:  M Virtanen; J Perheentupa; J Mäenpää; L Pitkänen; J Pikkarainen
Journal:  Eur J Pediatr       Date:  1984-11       Impact factor: 3.183

3.  Screening of the newborn for hypothyroidism.

Authors:  I M Rosenthal
Journal:  Indian J Pediatr       Date:  1982 Mar-Apr       Impact factor: 1.967

4.  Phenylketonuria (PKU) and the single gene: an old story retold.

Authors:  R M Murphey
Journal:  Behav Genet       Date:  1983-03       Impact factor: 2.805

5.  Fifteen-year experience with screening for phenylketonuria with an automated fluorometric method.

Authors:  H N Kirkman; C L Carroll; E G Moore; M S Matheson
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025
  5 in total

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