Literature DB >> 7474914

Transient neonatal hyperphenylalaninaemia is not related to mutations at the phenylalanine hydroxylase gene.

J Zschocke1, D J Carson.   

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Year:  1995        PMID： 7474914     DOI： 10.1007/bf00710439

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosis.

Authors:  J Zschocke; C A Graham; F J Stewart; D J Carson; N C Nevin
Journal:  Hum Mutat       Date:  1994       Impact factor: 4.878

2.  Hyperphenylalaninaemia of various types among three-quarters of a million neonates tested in a screening programme.

Authors:  V Walker; B E Clayton; R S Ersser; D E Francis; P Lilly; J W Seakins; I Smith; P D Whiteman
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791
  2 in total
  1 in total

1.  Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approach.

Authors:  J Zschocke; C A Graham; D J Carson; N C Nevin
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025
  1 in total

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