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 *

312 related articles for article (PubMed ID: 28982351)

  • 1. Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China.
    Liu N; Huang Q; Li Q; Zhao D; Li X; Cui L; Bai Y; Feng Y; Kong X
    BMC Med Genet; 2017 Oct; 18(1):108. PubMed ID: 28982351
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Analysis of PAH gene variants and prenatal diagnosis for 43 Chinese pedigrees affected with Phenylketonuria].
    Chai Y; Ning H; Xia J; Wang Y; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jun; 41(6):702-707. PubMed ID: 38818554
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation spectrum of PAH gene in phenylketonuria patients in Northwest China: identification of twenty novel variants.
    Yan Y; Zhang C; Jin X; Zhang Q; Zheng L; Feng X; Hao S; Gao H; Ma X
    Metab Brain Dis; 2019 Jun; 34(3):733-745. PubMed ID: 30747360
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutational spectrum of the phenylalanine hydroxylase gene in patients with phenylketonuria in the central region of China.
    Zhang Z; Gao JJ; Feng Y; Zhu LL; Yan H; Shi XF; Chang AM; Shi Y; Wang P
    Scand J Clin Lab Invest; 2018 May; 78(3):211-218. PubMed ID: 29390883
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Tianjin and surrounding areas of Northern China].
    Song L; Dang L; Meng Y; Fu B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb; 27(1):7-12. PubMed ID: 20140859
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Characteristics of PAH gene variants among 113 phenylketonuria patients from Henan Province].
    Chen C; Zhao Z; Ren Y; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):791-795. PubMed ID: 30512147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterisation of phenylketonuria in a Chinese mainland population using next-generation sequencing.
    Li N; Jia H; Liu Z; Tao J; Chen S; Li X; Deng Y; Jin X; Song J; Zhang L; Liang Y; Wang W; Zhu J
    Sci Rep; 2015 Oct; 5():15769. PubMed ID: 26503515
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mutation analysis of phenylalanine hydroxylase gene in 55 patients with phenylketonuria from Hebei province].
    Lu CX; Gao X; Wang JW; Zhang M; Zhu HW; Sun J; Xiao JF; Yang W; Zhao XL; Qi Z; Zhang X
    Zhonghua Yi Xue Za Zhi; 2011 Nov; 91(42):2971-6. PubMed ID: 22333022
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria in Shaanxi, China.
    Wang L; Wang X; He B; Cai N; Li W; Lou C; Xin S; Wu Q; Yu W; Qiang R
    J Pediatr Endocrinol Metab; 2017 Nov; 30(12):1305-1310. PubMed ID: 29176022
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The spectrum of phenylalanine hydroxylase variants and genotype-phenotype correlation in phenylketonuria patients in Gansu, China.
    Zhang C; Zhang P; Yan Y; Zhou B; Wang Y; Tian X; Hao S; Ma P; Zheng L; Zhang Q; Hui L; Wang Y; Cao Z; Ma X
    Hum Genomics; 2023 Apr; 17(1):36. PubMed ID: 37098607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [The mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Henan province].
    Wang FY; Shao CJ; Feng HG; Li CM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):644-9. PubMed ID: 21154324
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variations in genotype-phenotype correlations in phenylalanine hydroxylase deficiency in Chinese Han population.
    Zhu T; Ye J; Han L; Qiu W; Zhang H; Liang L; Gu X
    Gene; 2013 Oct; 529(1):80-7. PubMed ID: 23932990
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenylalanine hydroxylase deficiency in the Slovak population: genotype-phenotype correlations and genotype-based predictions of BH4-responsiveness.
    Polak E; Ficek A; Radvanszky J; Soltysova A; Urge O; Cmelova E; Kantarska D; Kadasi L
    Gene; 2013 Sep; 526(2):347-55. PubMed ID: 23764561
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational spectrum of phenylketonuria in the Chinese Han population: a novel insight into the geographic distribution of the common mutations.
    Zhu T; Qin S; Ye J; Qiu W; Han L; Zhang Y; Gu X
    Pediatr Res; 2010 Mar; 67(3):280-5. PubMed ID: 19915519
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Study of the phenylalanine hydroxylase gene variants in patients with phenylketonuria from Jiangxi province].
    Lu Q; Liu Y; Yang B; Xie K; Zou Y; Lu W; Wang F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Nov; 36(11):1057-1061. PubMed ID: 31703125
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Characteristics of the PAH gene mutation in Chinese patients with phenylketonuria in Xinjiang].
    Yu WZ; Qiu DH; Song F; Liu L; Liu SM; He XJ; Jin YW; Zhang YL; Zou HY; He J; Lei Q; Liu XW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):26-30. PubMed ID: 19199246
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutation analysis of the PAH gene in children with phenylketonuria from the Qinghai area of China].
    He J; Wang HZ; Xu FL; Yang X; Wang R; Zou HY; Yu WZ
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 Nov; 17(11):1221-7. PubMed ID: 26575882
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of Chinese families with phenylketonuria.
    Liu N; Kong XD; Zhao DH; Wu QH; Li XL; Guo HF; Cui LX; Jiang M; Shi HR
    Genet Mol Res; 2015 Nov; 14(4):14615-28. PubMed ID: 26600521
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. [Study on the mutations of phenylalanine hydroxylase gene in patients with phenylketonuria in Shanxi province].
    Gao WH; Zhang QB; Liu JP; Yang JP; Zhang GX; Ma YX; Zhang XG; Yu L; Zhou YA
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):393-6. PubMed ID: 21811977
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.