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 *

89 related articles for article (PubMed ID: 9758881)

  • 1. [Screening mutations in phenylketonuria by means of nonradioactive reverse dot blot hybridization].
    Yang T; Yuan L; Huang S; Zhao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):307-9. PubMed ID: 9758881
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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; 31(7):401-3. PubMed ID: 9275410
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [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; 16(1):9-11. PubMed ID: 9949232
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 21(3):261-3. PubMed ID: 15192831
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening for hereditary fructose intolerance mutations by reverse dot-blot.
    Lau J; Tolan DR
    Mol Cell Probes; 1999 Feb; 13(1):35-40. PubMed ID: 10024431
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

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

  • 9. [Comparison of genotype and intellectual phenotype in untreated phenylketonuric children].
    Yuan L; Fang B; Wang M; Wang T; Huang S; Yang T; Zhao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):297-9. PubMed ID: 9758878
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid detection of the R408W and I65T mutations in phenylketonuria by glycosylase mediated polymorphism detection.
    O'Donnell KA; Tighe O; O'Neill C; Naughten E; Mayne PD; McCarthy TV; Vaughan P; Croke DT
    Hum Mutat; 2001 May; 17(5):432. PubMed ID: 11317360
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Rapid diagnosis of non-deletion alpha-thalassemias by reverse dot blot].
    Li LY; Mo QH; Xu XM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):345-7. PubMed ID: 12903049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Frequency and distribution of phenylketonuric mutations in Orientals.
    Okano Y; Hase Y; Lee DH; Furuyama J; Shintaku H; Oura T; Isshiki G
    Hum Mutat; 1992; 1(3):216-20. PubMed ID: 1301927
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria model.
    Giannattasio S; Bisceglia L; Lattanzio P; Grifa A; Dianzani I; Gasparini P; Marra E
    Mol Cell Probes; 1995 Jun; 9(3):201-5. PubMed ID: 7477014
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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; 21(4):305-8. PubMed ID: 15300621
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR.
    Feriotto G; Ferlini A; Ravani A; Calzolari E; Mischiati C; Bianchi N; Gambari R
    Hum Mutat; 2001; 18(1):70-81. PubMed ID: 11438995
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid detection of PAH gene mutations in Chinese people.
    Zhang X; Chen HX; Li C; Zhang G; Liao SY; Peng ZC; Lai XP; Wang LL
    BMC Med Genet; 2019 Aug; 20(1):135. PubMed ID: 31382905
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Detecting rpoB gene mutation in rifampin-resistant Mycobacterium tuberculosis by using the reverse dot-blot hybridization method].
    Wang W; Pan W; Jin W; Weng X; Yan R; Su B; Chen S; Zhang W; Lu H; Qi Z
    Zhonghua Jie He He Hu Xi Za Zhi; 2002 Oct; 25(10):591-4. PubMed ID: 12490124
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany.
    Birk Møller L; Nygren AO; Scott P; Hougaard P; Bieber Nielsen J; Hartmann C; Güttler F; Tyfield L; Zschocke J
    Hum Mutat; 2007 Feb; 28(2):207. PubMed ID: 17221866
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Highly selective isolation of unknown mutations in diverse DNA fragments: toward new multiplex screening in cancer.
    Chakrabarti S; Price BD; Tetradis S; Fox EA; Zhang Y; Maulik G; Makrigiorgos GM
    Cancer Res; 2000 Jul; 60(14):3732-7. PubMed ID: 10919642
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.