BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

259 related articles for article (PubMed ID: 16638657)

  • 1. 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]  

  • 2. Positional cloning of a gene involved in hereditary multiple exostoses.
    Wuyts W; Van Hul W; Wauters J; Nemtsova M; Reyniers E; Van Hul EV; De Boulle K; de Vries BB; Hendrickx J; Herrygers I; Bossuyt P; Balemans W; Fransen E; Vits L; Coucke P; Nowak NJ; Shows TB; Mallet L; van den Ouweland AM; McGaughran J; Halley DJ; Willems PJ
    Hum Mol Genet; 1996 Oct; 5(10):1547-57. PubMed ID: 8894688
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.
    Wuyts W; Van Hul W; De Boulle K; Hendrickx J; Bakker E; Vanhoenacker F; Mollica F; Lüdecke HJ; Sayli BS; Pazzaglia UE; Mortier G; Hamel B; Conrad EU; Matsushita M; Raskind WH; Willems PJ
    Am J Hum Genet; 1998 Feb; 62(2):346-54. PubMed ID: 9463333
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses.
    Al-Zayed Z; Al-Rijjal RA; Al-Ghofaili L; BinEssa HA; Pant R; Alrabiah A; Al-Hussainan T; Zou M; Meyer BF; Shi Y
    Orphanet J Rare Dis; 2021 Feb; 16(1):100. PubMed ID: 33632255
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [A new EXT2 mutation in a Chinese family with hereditary multiple exostoses].
    Zhao WQ; Song SJ; Wei Q; Qiao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):241-4. PubMed ID: 19504431
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel mutation in the EXT-1 gene in an Iranian family affected with hereditary multiple exostoses.
    Foroughmand AM; Galehdari H; Rasouli M; Mohammadian G; Mohammadi M
    Pak J Biol Sci; 2008 Apr; 11(7):1037-41. PubMed ID: 18810975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel mutations of EXT1 and EXT2 genes among families and sporadic cases with multiple exostoses.
    Pei Y; Wang Y; Huang W; Hu B; Huang D; Zhou Y; Su P
    Genet Test Mol Biomarkers; 2010 Dec; 14(6):865-72. PubMed ID: 21039224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole-Exome Sequencing.
    Liang C; Wang YJ; Wei YX; Dong Y; Zhang ZC
    Orthop Surg; 2020 Jun; 12(3):990-996. PubMed ID: 32293802
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of Novel Mutations in the
    Tong Y; Zhang Y; Luo J; Hong Z; Chen X; Bi Q
    Genet Test Mol Biomarkers; 2021 Feb; 25(2):145-151. PubMed ID: 33596140
    [No Abstract]   [Full Text] [Related]  

  • 15. Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.
    Raskind WH; Conrad EU; Matsushita M; Wijsman EM; Wells DE; Chapman N; Sandell LJ; Wagner M; Houck J
    Hum Mutat; 1998; 11(3):231-9. PubMed ID: 9521425
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A splice mutation and mRNA decay of EXT2 provoke hereditary multiple exostoses.
    Tian C; Yan R; Wen S; Li X; Li T; Cai Z; Li X; Du H; Chen H
    PLoS One; 2014; 9(4):e94848. PubMed ID: 24728384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2.
    Kojima H; Wada T; Seki H; Kubota T; Wakui K; Fukushima Y
    Genet Test; 2008 Dec; 12(4):557-61. PubMed ID: 18976157
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-phenotype correlation in hereditary multiple exostoses.
    Francannet C; Cohen-Tanugi A; Le Merrer M; Munnich A; Bonaventure J; Legeai-Mallet L
    J Med Genet; 2001 Jul; 38(7):430-4. PubMed ID: 11432960
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.
    Ciavarella M; Coco M; Baorda F; Stanziale P; Chetta M; Bisceglia L; Palumbo P; Bengala M; Raiteri P; Silengo M; Caldarini C; Facchini R; Lala R; Cavaliere ML; De Brasi D; Pasini B; Zelante L; Guarnieri V; D'Agruma L
    Gene; 2013 Feb; 515(2):339-48. PubMed ID: 23262345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.
    Kang QL; Xu J; Zhang Z; He JW; Fu WZ; Zhang ZL
    Arch Med Res; 2013 Oct; 44(7):542-8. PubMed ID: 24120389
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.