Literature DB >> 7807959

Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients.

M Ozgüç1, E Yilmaz, H Erdem, T Coşkun, A Tokatli, I Ozalp.   

Abstract

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Year:  1994        PMID： 7807959     DOI： 10.1007/bf00711836

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


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  3 in total

1.  Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.

Authors:  A A Goltsov; R C Eisensmith; D S Konecki; U Lichter-Konecki; S L Woo
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

2.  Mutation analysis in Turkish phenylketonuria patients.

Authors:  M Ozgüç; I Ozalp; T Coşkun; E Yilmaz; H Erdem; S Ayter
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

3.  Multiple origins for phenylketonuria in Europe.

Authors:  R C Eisensmith; Y Okano; M Dasovich; T Wang; F Güttler; H Lou; P Guldberg; U Lichter-Konecki; D S Konecki; E Svensson
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025
  3 in total
  1 in total

1.  Association Between PAH Mutations and VNTR Alleles in the West Azerbaijani PKU Patients.

Authors:  Morteza Bagheri; Isa Abdi Rad; Nima Hosseini Jazani; Rasoul Zarrin; Ahad Ghazavi
Journal:  Maedica (Buchar)       Date:  2014-09
  1 in total

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