BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 10713884)

  • 21. [A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses].
    Xie ZG; Hu ZM; Pan Q; Zhang RF; Liang DS; Wu LQ; Long ZG; Dai HP; Xia K; Xia JH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):147-50. PubMed ID: 16604483
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes.
    Vujic M; Bergman A; Romanus B; Wahlström J; Martinsson T
    Int J Mol Med; 2004 Jan; 13(1):47-52. PubMed ID: 14654969
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.
    Philippe C; Porter DE; Emerton ME; Wells DE; Simpson AH; Monaco AP
    Am J Hum Genet; 1997 Sep; 61(3):520-8. PubMed ID: 9326317
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Identification of mutations in the human EXT1 and EXT2 genes].
    Song G; Zhou J; Xia J; Deng H; Xu L; Ruan Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Aug; 16(4):208-10. PubMed ID: 10431043
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutation screening of EXT genes in Chinese patients with multiple osteochondromas.
    Kang Z; Peng F; Ling T
    Gene; 2012 Sep; 506(2):298-300. PubMed ID: 22820392
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
    Vanita V; Sperling K; Sandhu HS; Sandhu PS; Singh JR
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):43-9. PubMed ID: 19309273
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Methylation status of EXT1 and EXT2 promoters and two mutations of EXT2 in chondrosarcoma.
    Tsuchiya T; Osanai T; Ogose A; Tamura G; Chano T; Kaneko Y; Ishikawa A; Orui H; Wada T; Ikeda T; Namba M; Takigawa M; Kawashima H; Hotta T; Tsuchiya A; Ogino T; Motoyama T
    Cancer Genet Cytogenet; 2005 Apr; 158(2):148-55. PubMed ID: 15796962
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutation analysis of hereditary multiple exostoses in the Chinese.
    Xu L; Xia J; Jiang H; Zhou J; Li H; Wang D; Pan Q; Long Z; Fan C; Deng HX
    Hum Genet; 1999; 105(1-2):45-50. PubMed ID: 10480354
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Reevaluation of a genetic model for the development of exostosis in hereditary multiple exostosis.
    Hall CR; Cole WG; Haynes R; Hecht JT
    Am J Med Genet; 2002 Sep; 112(1):1-5. PubMed ID: 12239711
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Molecular cloning of EXT2 and EXT4 gene].
    Deng H; Xu L; Ruan Q; Huang L; Xia J
    Hunan Yi Ke Da Xue Xue Bao; 1998; 23(6):519-23. PubMed ID: 10806756
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Three novel EXT1 and EXT2 gene mutations in Taiwanese patients with multiple exostoses.
    Chen WC; Chi CH; Chuang CC; Jou IM
    J Formos Med Assoc; 2006 May; 105(5):434-7. PubMed ID: 16638657
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A 651-665delinsTT mutation in EXT1 causes hereditary multiple exostoses.
    Shi YR; Wu JY; Tsai FJ; Lee CC; Tsai CH
    Hum Mutat; 2001 Feb; 17(2):158. PubMed ID: 11180615
    [No Abstract]   [Full Text] [Related]  

  • 33. Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.
    Shi YR; Wu JY; Hsu YA; Lee CC; Tsai CH; Tsai FJ
    Genet Test; 2002; 6(3):237-43. PubMed ID: 12490068
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses.
    Jamsheer A; Socha M; Sowińska-Seidler A; Telega K; Trzeciak T; Latos-Bieleńska A
    J Appl Genet; 2014 May; 55(2):183-8. PubMed ID: 24532482
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Evaluation of the anatomic burden of patients with hereditary multiple exostoses.
    Alvarez CM; De Vera MA; Heslip TR; Casey B
    Clin Orthop Relat Res; 2007 Sep; 462():73-9. PubMed ID: 17589361
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation screening of the BRCA1 gene in Slovak patients.
    Tomka M; Sedlakova O; Reinerova M; Veselovska Z; Stevurková V; Bartosová Z; Zajac V
    Neoplasma; 2001; 48(6):451-5. PubMed ID: 11949836
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical outcome and genotype in patients with hereditary multiple exostoses.
    Jäger M; Westhoff B; Portier S; Leube B; Hardt K; Royer-Pokora B; Gossheger G; Krauspe R
    J Orthop Res; 2007 Dec; 25(12):1541-51. PubMed ID: 17676624
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis).
    Faiyaz-Ul-Haque M; Ahmad W; Zaidi SH; Hussain S; Haque S; Ahmad M; Cohn DH; Tsui LC
    Clin Genet; 2004 Aug; 66(2):144-51. PubMed ID: 15253765
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis.
    Bénit P; Bonnefont JP; Kara Mostefa A; Francannet C; Munnich A; Ray PF
    Prenat Diagn; 2001 Apr; 21(4):279-83. PubMed ID: 11288117
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Comparison of SSCP and DHPLC for the detection of LDLR mutations in a New Zealand cohort.
    Bunn CF; Lintott CJ; Scott RS; George PM
    Hum Mutat; 2002 Mar; 19(3):311. PubMed ID: 11857755
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.