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 *

202 related articles for article (PubMed ID: 8104860)

  • 1. Phenylketonuria in Spain: RFLP haplotypes and linked mutations.
    Desviat LR; Pérez B; Ugarte M
    Hum Genet; 1993 Oct; 92(3):254-8. PubMed ID: 8104860
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families.
    Kozák L; Kuhrová V; Blazková M; Romano V; Fajkusová L; Dvoráková D; Pijácková A
    Hum Genet; 1995 Oct; 96(4):472-6. PubMed ID: 7557973
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal.
    Rivera I; Leandro P; Lichter-Konecki U; Tavares de Almeida I; Lechner MC
    J Med Genet; 1998 Apr; 35(4):301-4. PubMed ID: 9598724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families.
    Meijer H; Jongbloed RJ; Hekking M; Spaapen LJ; Geraedts JP
    Hum Genet; 1993 Dec; 92(6):588-92. PubMed ID: 7903270
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of phenylketonuria alleles in the Italian population.
    Dianzani I; Giannattasio S; de Sanctis L; Alliaudi C; Lattanzio P; Dionisi Vici C; Burlina A; Burroni M; Sebastio G; Carnevale F
    Eur J Hum Genet; 1995; 3(5):294-302. PubMed ID: 8556304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Relative frequency, heterogeneity and geographic clustering of PKU mutations in Norway.
    Eiken HG; Knappskog PM; Boman H; Thune KS; Kaada G; Motzfeldt K; Apold J
    Eur J Hum Genet; 1996; 4(4):205-13. PubMed ID: 8875186
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 'Celtic' phenylketonuria chromosomes found? Evidence in two regions of Quebec Province.
    Treacy E; Byck S; Clow C; Scriver CR
    Eur J Hum Genet; 1993; 1(3):220-8. PubMed ID: 7913864
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum and origin of phenylketonuria mutations in Spain.
    Pérez B; Desviat LR; De Lucca M; Ugarte M
    Acta Paediatr Suppl; 1994 Dec; 407():34-6. PubMed ID: 7766951
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy.
    Dianzani I; Devoto M; Camaschella C; Saglio G; Ferrero GB; Cerone R; Romano C; Romeo G; Giovannini M; Riva E
    Hum Genet; 1990 Nov; 86(1):69-72. PubMed ID: 1979309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal.
    Caillaud C; Vilarinho L; Vilarinho A; Rey F; Berthelon M; Santos R; Lyonnet S; Briard ML; Osorio RV; Rey J
    Hum Genet; 1992 Apr; 89(1):69-72. PubMed ID: 1349566
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PKU in Slovakia: mutation screening and haplotype analysis.
    Kádasi L; Poláková H; Feráková E; Hudecová S; Bohusová T; Szomolayová I; Strnová J; Hruskovic I; Moschonas NK; Ferák V
    Hum Genet; 1995 Jan; 95(1):112-4. PubMed ID: 7814013
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutations.
    Kalaydjieva L; Dworniczak B; Aulehla-Scholz C; Kremensky I; Bronzova J; Eigel A; Horst J
    J Med Genet; 1990 Dec; 27(12):742-5. PubMed ID: 1981599
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations.
    Kozák L; Blazková M; Kuhrová V; Pijácková A; Růzicková S; St'astná S
    J Med Genet; 1997 Nov; 34(11):893-8. PubMed ID: 9391881
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.
    Svensson E; von Döbeln U; Hagenfeldt L
    Hum Genet; 1991 May; 87(1):11-7. PubMed ID: 1674714
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU).
    Daiger SP; Chakraborty R; Reed L; Fekete G; Schuler D; Berenssi G; Nasz I; Brdicka R; Kamarýt J; Pijácková A
    Am J Hum Genet; 1989 Aug; 45(2):310-8. PubMed ID: 2569271
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.
    DiLella AG; Marvit J; Brayton K; Woo SL
    Nature; 1987 May 28-Jun 3; 327(6120):333-6. PubMed ID: 2884570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of PKU in Ireland.
    O'Neill CA; Eisensmith RC; Croke DT; Naughten ER; Cahalane SF; Woo SL
    Acta Paediatr Suppl; 1994 Dec; 407():43-4. PubMed ID: 7766956
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of the phenylalanine hydroxylase gene in the Spanish population: mutation profile and association with intragenic polymorphic markers.
    Pérez B; Desviat LR; Ugarte M
    Am J Hum Genet; 1997 Jan; 60(1):95-102. PubMed ID: 8981952
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.