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.
89 related articles for article (PubMed ID: 7915167)
21. [Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria]. Zhang J; Meng J; Zhai X; Fang G; Gao J; Shi M; Wang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):134-7. PubMed ID: 15793771 [TBL] [Abstract][Full Text] [Related]
22. [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; 36(6):849-52. PubMed ID: 10923269 [TBL] [Abstract][Full Text] [Related]
24. Detection of point mutations of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria. Fang B; Yuan L; Wang M; Huang S; Wang T; Miao S; Ye J; Sun N; Lo H; Savio LC Chin Med Sci J; 1992 Dec; 7(4):205-8. PubMed ID: 1307495 [TBL] [Abstract][Full Text] [Related]
25. Polymorphism in the 3' untranslated region of the phenylalanine hydroxylase gene detected by enzyme mismatch cleavage: evolution of haplotypes. Ramus SJ; Cotton RG Hum Genet; 1995 Dec; 96(6):741-3. PubMed ID: 8522340 [TBL] [Abstract][Full Text] [Related]
26. Molecular analysis of the phenylalanine hydroxylase gene in Mexican phenylketonuric patients. Nicolini H; Cruz C; Camarena B; Fernanda Merino M; Bilbao G; Vela M; Velázquez A; Pérez B; Desviat L; Ugarte M Arch Med Res; 1995; 26(1):53-7. PubMed ID: 7711448 [TBL] [Abstract][Full Text] [Related]
27. [Spectrum and methods of detection of mutations in a phenylalanine hydroxylase gene from patients with phenylketonuria from the Novosibirsk region]. Smagulova FO; Morozov IV Bioorg Khim; 2000 Nov; 26(11):838-43. PubMed ID: 11696894 [TBL] [Abstract][Full Text] [Related]
28. [Molecular genetic aspects of phenylketonuria (PKU)]. Giltay JC; van Hoef AM; de Weger R; Duran M; Berger R; Beemer FA Tijdschr Kindergeneeskd; 1991 Jun; 59(3):77-80. PubMed ID: 1677790 [TBL] [Abstract][Full Text] [Related]
29. Analysis of exon 7 of the human phenylalanine hydroxylase gene: a mutation hot spot? Dworniczak B; Kalaydjieva L; Pankoke S; Aulehla-Scholz C; Allen G; Horst J Hum Mutat; 1992; 1(2):138-46. PubMed ID: 1363786 [TBL] [Abstract][Full Text] [Related]
30. Inactivation of phenylalanine hydroxylase by a missense mutation, R270S, in a Palestinian kinship with phenylketonuria. Kleiman S; Li J; Schwartz G; Eisensmith RC; Woo SL; Shiloh Y Hum Mol Genet; 1993 May; 2(5):605-6. PubMed ID: 8518802 [No Abstract] [Full Text] [Related]
31. Gypsy phenylketonuria: a point mutation of the phenylalanine hydroxylase gene in Gypsy families from Slovakia. Kalanin J; Takarada Y; Kagawa S; Yamashita K; Ohtsuka N; Matsuoka A Am J Med Genet; 1994 Jan; 49(2):235-9. PubMed ID: 8116675 [TBL] [Abstract][Full Text] [Related]
32. Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan. Okano Y; Kudo S; Nishi Y; Sakaguchi T; Aso K J Hum Genet; 2011 Apr; 56(4):306-12. PubMed ID: 21307867 [TBL] [Abstract][Full Text] [Related]
33. [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; 43(4):20-4. PubMed ID: 19938643 [TBL] [Abstract][Full Text] [Related]
34. Characterization of the mouse phenylalanine hydroxylase mutation Pah(enu3). Haefele MJ; White G; McDonald JD Mol Genet Metab; 2001 Jan; 72(1):27-30. PubMed ID: 11161825 [TBL] [Abstract][Full Text] [Related]
35. Identification of seven new mutations in the phenylalanine hydroxylase gene, associated with hyperphenylalaninemia in the Belgian population. Michiels L; François B; Raus J; Vandevyver C Hum Mutat; 1998; Suppl 1():S123-4. PubMed ID: 9452062 [No Abstract] [Full Text] [Related]
36. Novel mutation identified in the PAH gene. Charikova EV Hum Hered; 1996; 46(1):36-40. PubMed ID: 8825461 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. Identification of two new phenylalanine hydroxylase alleles in Sicilian phenylketonuric families. Romano V; Ceratto N; Chiavetta V; Bosco P J Inherit Metab Dis; 1993; 16(3):599-601. PubMed ID: 7609461 [No Abstract] [Full Text] [Related]
39. 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]
40. Phenylketonuria in China: identification and characterization of three novel nucleotide substitutions in the human phenylalanine hydroxylase gene. Li J; Eisensmith RC; Wang T; Lo WH; Huang SZ; Zeng YT; Yuan LF; Liu SR; Woo SL Hum Mutat; 1994; 3(3):312-4. PubMed ID: 8019568 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]