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403 related items for PubMed ID: 12655551

  • 1. The molecular basis of phenylketonuria in Latvia.
    Pronina N, Giannattasio S, Lattanzio P, Lugovska R, Vevere P, Kornejeva A.
    Hum Mutat; 2003 Apr; 21(4):398-9. PubMed ID: 12655551
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  • 2. The molecular basis of phenylketonuria in Lithuania.
    Kasnauskiene J, Giannattasio S, Lattanzio P, Cimbalistiene L, Kucinskas V.
    Hum Mutat; 2003 Apr; 21(4):398. PubMed ID: 12655550
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  • 3. Frequencies of the most common mutations responsible for phenylketonuria in Poland.
    Zekanowski C, Nowacka M, Zgulska M, Horst J, Cabalska B, Mazurczak T.
    Mol Cell Probes; 1994 Aug; 8(4):323-4. PubMed ID: 7870074
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  • 5. [Screening for mutation variants in exons 5, 7, 12 of phenylalanine hydroxylase gene using denaturing gradient gel-electrophoresis].
    Solovĭov OO, Livshyts' LA.
    Tsitol Genet; 2009 Aug; 43(4):20-4. PubMed ID: 19938643
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  • 6. The molecular basis of phenylalanine hydroxylase deficiency in Croatia.
    Zschocke J, Preusse A, Sarnavka V, Fumic K, Mardesic D, Hoffmann GF, Baric I.
    Hum Mutat; 2003 Apr; 21(4):399. PubMed ID: 12655552
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  • 7. PKU in Minas Gerais State, Brazil: mutation analysis.
    Santos LL, Castro-Magalhães M, Fonseca CG, Starling AL, Januário JN, Aguiar MJ, Carvalho MR.
    Ann Hum Genet; 2008 Nov; 72(Pt 6):774-9. PubMed ID: 18798839
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  • 8. Mutation spectrum of the PAH gene in the PKU patients from Khorasan Razavi province of Iran.
    Hamzehloei T, Hosseini SA, Vakili R, Mojarad M.
    Gene; 2012 Sep 10; 506(1):230-2. PubMed ID: 22763404
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  • 12. [Mutation in the structure of exon 7 of the phenylalanine hydroxylase in phenylketonuria patients from the Novosibirsk area].
    Smagulova FO, Maslennikov AB, Morozov IV, Kitaĭnik GP.
    Genetika; 2000 Jun 10; 36(6):849-52. PubMed ID: 10923269
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  • 13. Mutation screening of phenylketonuria in the Far East of Russia.
    Sueoka H, Moshinetsky A, Nagao M, Chiba S.
    J Hum Genet; 1999 Jun 10; 44(6):368-71. PubMed ID: 10570906
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  • 14. Phenylketonuria: genotype-phenotype correlations based on expression analysis of structural and functional mutations in PAH.
    Pey AL, Desviat LR, Gámez A, Ugarte M, Pérez B.
    Hum Mutat; 2003 Apr 10; 21(4):370-8. PubMed ID: 12655546
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  • 16. Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil.
    Santos LL, Magalhães Mde C, Reis Ade O, Starling AL, Januário JN, Fonseca CG, Aguiar MJ, Carvalho MR.
    Genet Mol Res; 2006 Mar 31; 5(1):16-23. PubMed ID: 16755493
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  • 17. [Spectrum of phenylalanine hydroxylase gene mutations and genotype-phenotype correlation in the patients with phenylketonuria in Beijing area of China].
    Qu YJ, Song F, Jin YW, Wang H, Zhang YM, Qin JL, Qiu L.
    Zhonghua Er Ke Za Zhi; 2008 Feb 31; 46(2):115-9. PubMed ID: 19099685
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  • 20. Predicting a clinical/biochemical phenotype for PKU/MHP patients with PAH gene mutations.
    Kasnauskiene J, Cimbalistiene L, Kucinskas V.
    Genetika; 2008 Oct 31; 44(10):1397-403. PubMed ID: 19062537
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