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248 related items for PubMed ID: 9575658

  • 1. [Novel mutations identified in exon 7 of phenylalanine hydroxylase gene in Chinese].
    Sun G, Jiang L, Zhang X, Tong B, Dong G, Sun K.
    Yi Chuan Xue Bao; 1997; 24(6):492-5. PubMed ID: 9575658
    [Abstract] [Full Text] [Related]

  • 2. Mutations identified in exon 7 of phenylalanine hydroxylase gene in Chinese.
    Sun G, Jiang L, Zhang X, Tong B, Dong G, Sun K.
    Chin Med Sci J; 1997 Sep; 12(3):156-8. PubMed ID: 11360625
    [Abstract] [Full Text] [Related]

  • 3. [Identification of mutations in the phenylalanine hydroxylase gene and exon 5 novel mutation Y166X(C-->G) in Yunnan].
    Wang N, Zhu Y, Xu K, Qiu Z, Song W, Huang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Feb 10; 16(1):9-11. PubMed ID: 9949232
    [Abstract] [Full Text] [Related]

  • 4. [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 10; 22(2):134-7. PubMed ID: 15793771
    [Abstract] [Full Text] [Related]

  • 5. [Ten novel mutations in the phenylalanine hydroxylase gene identified in Chinese patients with phenylketonuria].
    Song F, Jin YW, Wang H, Yang YL, Zhang YM, Zhang T.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Apr 10; 25(2):142-4. PubMed ID: 12905706
    [Abstract] [Full Text] [Related]

  • 6. [Study on mutations of exon 12 of the PAH gene in 127 phenylketonuria patients].
    Qiu WJ, Zhang YF, Ye J, Han LS, Gu XF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun 10; 21(3):261-3. PubMed ID: 15192831
    [Abstract] [Full Text] [Related]

  • 7. [Six novel mutations in PAH gene detected by sequencing].
    Zhang Z, He YS, Peng SX, Wang FH, Jiang JH, Jing RJ, Cheng G, Xu J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug 10; 21(4):305-8. PubMed ID: 15300621
    [Abstract] [Full Text] [Related]

  • 8. Phenylketonuria mutations in Northern China.
    Song F, Qu YJ, Zhang T, Jin YW, Wang H, Zheng XY.
    Mol Genet Metab; 2005 Dec 10; 86 Suppl 1():S107-18. PubMed ID: 16256386
    [Abstract] [Full Text] [Related]

  • 9. [Analysis of mutations in exon 7 of phenylalanine hydroxylase gene among children with phenylketonuria in Ningxia, China].
    Mao XM, He J, Liu Y, Li XQ, Yu WZ, Gao ZH, Cai J.
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Mar 10; 16(3):259-62. PubMed ID: 24661517
    [Abstract] [Full Text] [Related]

  • 10. [Screening for mutations in the PAH gene in Chinese: a new splice and a novel polymorphic mutation].
    Xu L, Miao S, Liu G.
    Zhonghua Yi Xue Za Zhi; 1996 Jun 10; 76(6):451-4. PubMed ID: 9275491
    [Abstract] [Full Text] [Related]

  • 11. [Analysis of RFLP haplotypes and point mutations at the phenylalanine hydroxylase (PAH) locus in PKU families from north China].
    Fang B.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb 10; 14(1):46-50. PubMed ID: 1350519
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria.
    Acosta A, Silva W, Carvalho T, Gomes M, Zago M.
    Hum Mutat; 2001 Feb 10; 17(2):122-30. PubMed ID: 11180595
    [Abstract] [Full Text] [Related]

  • 14. [Mutation analysis of the PAH gene in patients with phenylketonuria in Gansu province].
    Yan YS, Wang Z, Hao SJ, Meng Y, Zheng L, Huang SZ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug 10; 26(4):419-22. PubMed ID: 20017307
    [Abstract] [Full Text] [Related]

  • 15. Molecular analysis of phenylketonuria (PKU) in newborns from Texas.
    Yang Y, Drummond-Borg M, Garcia-Heras J.
    Hum Mutat; 2001 Jun 10; 17(6):523. PubMed ID: 11385716
    [Abstract] [Full Text] [Related]

  • 16. [Detection of the mutational gene in phenylketonuria and prenatal diagnoses by using single strand conformation polymorphism methods].
    Yang T, Yuan L, Huang S.
    Zhonghua Fu Chan Ke Za Zhi; 1996 Jul 10; 31(7):401-3. PubMed ID: 9275410
    [Abstract] [Full Text] [Related]

  • 17. [Correlation between genotypes and biochemical phenotypes of phenylalanine hydroxylase in patients with phenylketonuria].
    Shu JB, Meng YT, Dang LH, Fu BJ, Song L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec 10; 29(6):635-41. PubMed ID: 23225039
    [Abstract] [Full Text] [Related]

  • 18. [Frequencies of 6 known mutations in phenylalanine hydroxylase gene and their application in prenatal gene diagnosis].
    Wang M.
    Zhonghua Yi Xue Za Zhi; 1992 Nov 10; 72(11):670-3, 702-3. PubMed ID: 1338705
    [Abstract] [Full Text] [Related]

  • 19. The importance of arginine mutation for the evolutionary structure and function of phenylalanine hydroxylase gene.
    Lüleyap HU, Alptekin D, Pazarbaşi A, Kasap M, Kasap H, Demirhindi H, Mungan N, Ozer G, Froster UG.
    Mutat Res; 2006 Oct 10; 601(1-2):39-45. PubMed ID: 16765994
    [Abstract] [Full Text] [Related]

  • 20. [Mutations in exon 7 of the phenylalanine hydroxylase (PAH) gene in chinese patients with phenylketonuria].
    Song F, Jin YW, Wang H, Zhang YM, Yang YL, Zhang T.
    Yi Chuan; 2005 Jan 10; 27(1):53-6. PubMed ID: 15730960
    [Abstract] [Full Text] [Related]

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