These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

92 related articles for article (PubMed ID: 7807959)

  • 1. Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients.
    Ozgüç M; Yilmaz E; Erdem H; Coşkun T; Tokatli A; Ozalp I
    J Inherit Metab Dis; 1994; 17(3):373-4. PubMed ID: 7807959
    [No Abstract]   [Full Text] [Related]  

  • 2. Phenylketonuria mutations in Germany.
    Zschocke J; Hoffmann GF
    Hum Genet; 1999 May; 104(5):390-8. PubMed ID: 10394930
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg.
    Baranovskaya S; Shevtsov S; Maksimova S; Kuzmin A; Schwartz E
    J Inherit Metab Dis; 1996; 19(5):705. PubMed ID: 8892033
    [No Abstract]   [Full Text] [Related]  

  • 4. Molecular Genetic Analysis of the Variable Number of Tandem-Repeat Alleles at the Phenylalanine Hydroxylase Gene in Iranian Azeri Turkish Population.
    Bagheri M; Abdi Rad I; Hosseini Jazani N; Zarrin R; Ghazavi A
    Iran Biomed J; 2015; 19(3):183-7. PubMed ID: 26025954
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients.
    Ozgüç M; Ozalp I; Coşkun T; Yilmaz E; Erdem H; Ayter S
    Turk J Pediatr; 1993; 35(1):11-4. PubMed ID: 7901929
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation analysis in Turkish phenylketonuria patients.
    Ozgüç M; Ozalp I; Coşkun T; Yilmaz E; Erdem H; Ayter S
    J Med Genet; 1993 Feb; 30(2):129-30. PubMed ID: 8445616
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carrier detection of phenylketonuria in Iranian families by variable number tandem-repeat polymorphism analysis.
    Hosseini-Mazinani SM; Koochmeshgi J; Khazaee-Koohpar Z; Hosein-Pur-Nobari N; Seifati SM
    East Mediterr Health J; 2008; 14(6):1445-51. PubMed ID: 19161120
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenylketonuria mutations and linked haplotypes in the Lithuanian population: origin of the most common R408W mutation.
    Giannattasio S; Jurgelevicius V; Lattanzio P; Cimbalistienè L; Marra E; Kucinskas V
    Hum Hered; 1997; 47(3):155-60. PubMed ID: 9156326
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.
    Stuhrmann M; Riess O; Mönch E; Kurdoglu G
    Clin Genet; 1989 Aug; 36(2):117-21. PubMed ID: 2569949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuria.
    Bonyadi M; Omrani O; Moghanjoghi SM; Shiva S
    Genet Test Mol Biomarkers; 2010 Apr; 14(2):233-5. PubMed ID: 20187763
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The identification of two mis-sense mutations at the PAH gene locus in a Turkish patient with phenylketonuria.
    Konecki DS; Schlotter M; Trefz FK; Lichter-Konecki U
    Hum Genet; 1991 Aug; 87(4):389-93. PubMed ID: 1679030
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples.
    Calì F; Dianzani I; Desviat LR; Perez B; Ugarte M; Ozguc M; Seyrantepe V; Shiloh Y; Giannattasio S; Carducci C; Bosco P; De Leo G; Piazza A; Romano V
    Hum Genet; 1997 Sep; 100(3-4):350-5. PubMed ID: 9272154
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations.
    Byck S; Morgan K; Tyfield L; Dworniczak B; Scriver CR
    Hum Mol Genet; 1994 Sep; 3(9):1675-7. PubMed ID: 7833927
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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; 46(2):115-9. PubMed ID: 19099685
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation screening of phenylketonuria in the Far East of Russia.
    Sueoka H; Moshinetsky A; Nagao M; Chiba S
    J Hum Genet; 1999; 44(6):368-71. PubMed ID: 10570906
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of mutations and VNTR-polymorphism in the phenylalanine hydroxylase gene].
    Hechyporenko MV; Kravchenko SA; Livshyts LA
    Ukr Biokhim Zh (1999); 2001; 73(2):63-7. PubMed ID: 11642047
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic diversity within the R408W phenylketonuria mutation lineages in Europe.
    Tighe O; Dunican D; O'Neill C; Bertorelle G; Beattie D; Graham C; Zschocke J; Cali F; Romano V; Hrabincova E; Kozak L; Nechyporenko M; Livshits L; Guldberg P; Jurkowska M; Zekanowski C; Perez B; Desviat LR; Ugarte M; Kucinskas V; Knappskog P; Treacy E; Naughten E; Tyfield L; Byck S; Scriver CR; Mayne PD; Croke DT
    Hum Mutat; 2003 Apr; 21(4):387-93. PubMed ID: 12655548
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles.
    Popescu T; Blazkova M; Kozak L; Jebeleanu G; Popescu A
    Hum Mutat; 1998; 12(5):314-9. PubMed ID: 9792407
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population.
    Dobrowolski SF; Heintz C; Miller T; Ellingson C; Ellingson C; Ozer I; Gökçay G; Baykal T; Thöny B; Demirkol M; Blau N
    Mol Genet Metab; 2011 Feb; 102(2):116-21. PubMed ID: 21147011
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation Analysis in Classical Phenylketonuria Patients Followed by Detecting Haplotypes Linked to Some PAH Mutations.
    Dehghanian F; Silawi M; Tabei SM
    Clin Lab; 2017 Feb; 63(2):295-300. PubMed ID: 28182360
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.