BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 32293802)

  • 21. [Mutation analysis of EXT genes in two pedigrees with hereditary multiple exostoses].
    Deng LB; Quan Y; Liu J; Lin Peng SY; Liang DS; Wu LQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):641-4. PubMed ID: 24327137
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Identification of four novel EXT1 and EXT2 mutations in five Chinese pedigrees with hereditary multiple exostoses.
    Li Y; Wang D; Wang W; Wang J; Li H; Wang J; Wang X; Fu Q
    Genet Test Mol Biomarkers; 2009 Dec; 13(6):825-30. PubMed ID: 19839753
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.
    Li Y; Lin X; Zhu M; Li J; Yuan Z; Xu H
    Mol Med Rep; 2020 Sep; 22(3):2469-2477. PubMed ID: 32705272
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Heterogeneous spectrum of EXT gene mutations in Chinese patients with hereditary multiple osteochondromas.
    Li Y; Wang J; Tang J; Wang Z; Han B; Li N; Yu T; Chen Y; Fu Q
    Medicine (Baltimore); 2018 Oct; 97(42):e12855. PubMed ID: 30334991
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Analysis of mutations in EXT1 and EXT2 in Brazilian patients with multiple osteochondromas.
    Santos SCL; Rizzo IMPO; Takata RI; Speck-Martins CE; Brum JM; Sollaci C
    Mol Genet Genomic Med; 2018 May; 6(3):382-392. PubMed ID: 29529714
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis].
    Lou G; Yang K; Qin L; Zhang Y; Wang H; Hou Q; He M; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):91-95. PubMed ID: 29419870
    [TBL] [Abstract][Full Text] [Related]  

  • 30. New mutations of EXT1 and EXT2 genes in German patients with Multiple Osteochondromas.
    Heinritz W; Hüffmeier U; Strenge S; Miterski B; Zweier C; Leinung S; Bohring A; Mitulla B; Peters U; Froster UG
    Ann Hum Genet; 2009 May; 73(Pt 3):283-91. PubMed ID: 19344451
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic and functional analyses detect an EXT1 splicing pathogenic variant in a Chinese hereditary multiple exostosis (HME) family.
    Li J; Wang Z; Han Y; Jin C; Cheng D; Zhou YA; Zhen J
    Mol Genet Genomic Med; 2022 Mar; 10(3):e1878. PubMed ID: 35106951
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases.
    Lonie L; Porter DE; Fraser M; Cole T; Wise C; Yates L; Wakeling E; Blair E; Morava E; Monaco AP; Ragoussis J
    Hum Mutat; 2006 Nov; 27(11):1160. PubMed ID: 17041877
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas.
    Pedrini E; De Luca A; Valente EM; Maini V; Capponcelli S; Mordenti M; Mingarelli R; Sangiorgi L; Dallapiccola B
    Hum Mutat; 2005 Sep; 26(3):280. PubMed ID: 16088908
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Screening for EXT1 and EXT2 gene mutations in a ethnic Han Chinese family from Shanxi with hereditary multiple exostoses].
    Zhou YA; Ma YX; Zhang YH; Hao ZQ; Li XJ; Shi YY; Zhang QB; Li PL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):95-8. PubMed ID: 23450490
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Exome sequencing and functional analysis identifies a novel mutation in EXT1 gene that causes multiple osteochondromas.
    Zhang F; Liang J; Guo X; Zhang Y; Wen Y; Li Q; Zhang Z; Ma W; Dai L; Liu X; Yang L; Wang J
    PLoS One; 2013; 8(8):e72316. PubMed ID: 24009674
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses.
    Seki H; Kubota T; Ikegawa S; Haga N; Fujioka F; Ohzeki S; Wakui K; Yoshikawa H; Takaoka K; Fukushima Y
    Am J Med Genet; 2001 Feb; 99(1):59-62. PubMed ID: 11170095
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family.
    Ajmal M; Muhammad H; Nasir M; Shoaib M; Malik SA; Ullah I
    Medicina (Kaunas); 2022 Dec; 59(1):. PubMed ID: 36676722
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. Mutation analysis and prenatal diagnosis of EXT1 gene mutations in Chinese patients with multiple osteochondromas.
    Zhu HY; Hu YL; Yang Y; Wu X; Zhu RF; Zhu XY; Duan HL; Zhang Y; Zhou JY
    Chin Med J (Engl); 2011 Oct; 124(19):3054-7. PubMed ID: 22040554
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.