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 *

174 related articles for article (PubMed ID: 30719288)

  • 1. Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome.
    Luong ALT; Ho TT; Hoang H; Nguyen TQ; Ho TC; Tran PD; Hoang TT; Nguyen NT; Chu HH
    Biomed Rep; 2019 Feb; 10(2):107-112. PubMed ID: 30719288
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited FGFR2 mutation in a Chinese patient with Crouzon syndrome and luxation of bulbus oculi provoked by trauma: a case report.
    Yang J; Tao T; Liu H; Hu ZL
    BMC Ophthalmol; 2019 Oct; 19(1):209. PubMed ID: 31640617
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome.
    Fan J; Li Y; Jia R; Fan X
    BMC Med Genet; 2018 May; 19(1):91. PubMed ID: 29848297
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FGFR2 molecular analysis and related clinical findings in one Chinese family with Crouzon syndrome.
    Lin Y; Liang X; Ai S; Chen C; Liu X; Luo L; Ye S; Li B; Liu Y; Yang H
    Mol Vis; 2012; 18():449-54. PubMed ID: 22355256
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ala344Pro mutation in the FGFR2 gene and related clinical findings in one Chinese family with Crouzon syndrome.
    Lin Y; Ai S; Chen C; Liu X; Luo L; Ye S; Liang X; Zhu Y; Yang H; Liu Y
    Mol Vis; 2012; 18():1278-82. PubMed ID: 22665975
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of FGFR 2 and associated clinical observations in two Chinese families with Crouzon syndrome.
    Lin Y; Gao H; Ai S; Eswarakumar JV; Li T; Liu B; Jiang H; Liu Y; Liu X; Li Y; Ni Y; Chen J; Lin Z; Liang X; Jin C; Huang X; Lu L; Liu Y
    Mol Med Rep; 2016 Sep; 14(3):1941-6. PubMed ID: 27430617
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.
    Lin M; Lu Y; Sui Y; Zhao N; Jin Y; Yi D; Jiang M
    Mol Genet Genomic Med; 2019 Sep; 7(9):e843. PubMed ID: 31318164
    [TBL] [Abstract][Full Text] [Related]  

  • 8. C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.
    Lin Y; Gao H; Ai S; Eswarakumar JVP; Chen C; Zhu Y; Li T; Liu B; Liu X; Luo L; Jiang H; Li Y; Liang X; Jin C; Huang X; Lu L
    Mol Med Rep; 2017 Oct; 16(4):5333-5337. PubMed ID: 28849010
    [TBL] [Abstract][Full Text] [Related]  

  • 9. FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome.
    Lin Y; Gao H; Ai S; Eswarakumar JVP; Zhu Y; Chen C; Li T; Liu B; Jiang H; Liu Y; Li Y; Wu Q; Li H; Liang X; Jin C; Huang X; Lu L
    Mol Med Rep; 2017 Nov; 16(5):5841-5846. PubMed ID: 28901406
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome: A case report.
    Shi H; Yang J; Guo Q; Zhang M
    Medicine (Baltimore); 2021 Mar; 100(10):e24991. PubMed ID: 33725872
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [FGFR2 gene mutation in a family with Crouzon syndrome and a sporadic Crouzon syndrome patient].
    Guo L; Lai YN; Li LX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):218-20. PubMed ID: 18393251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome.
    Gorry MC; Preston RA; White GJ; Zhang Y; Singhal VK; Losken HW; Parker MG; Nwokoro NA; Post JC; Ehrlich GD
    Hum Mol Genet; 1995 Aug; 4(8):1387-90. PubMed ID: 7581378
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal exclusion of Crouzon syndrome by mutation analysis of FGFR2.
    Phupong V; Srichomthong C; Shotelersuk V
    Southeast Asian J Trop Med Public Health; 2004 Dec; 35(4):977-9. PubMed ID: 15916101
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance.
    Everett ET; Britto DA; Ward RE; Hartsfield JK
    Cleft Palate Craniofac J; 1999 Nov; 36(6):533-41. PubMed ID: 10574673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing.
    Meyers GA; Day D; Goldberg R; Daentl DL; Przylepa KA; Abrams LJ; Graham JM; Feingold M; Moeschler JB; Rawnsley E; Scott AF; Jabs EW
    Am J Hum Genet; 1996 Mar; 58(3):491-8. PubMed ID: 8644708
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.
    Liu J; Nam HK; Wang E; Hatch NE
    Calcif Tissue Int; 2013 May; 92(5):451-66. PubMed ID: 23358860
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Li ZL; Chen X; Zhuang WJ; Zhao W; Liu YN; Zhang FX; Ha RS; Wu JH; Zhao C; Sheng XL
    Int J Ophthalmol; 2016; 9(10):1403-1408. PubMed ID: 27803855
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First-trimester prenatal diagnosis of Crouzon syndrome.
    Schwartz M; Kreiborg S; Skovby F
    Prenat Diagn; 1996 Feb; 16(2):155-8. PubMed ID: 8650126
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular diagnosis of bilateral coronal synostosis.
    Mulliken JB; Steinberger D; Kunze S; Müller U
    Plast Reconstr Surg; 1999 Nov; 104(6):1603-15. PubMed ID: 10541159
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Analysis of FGFR2 gene mutations in two Chinese families with Crouzon syndrome].
    Huang Y; Mei L; Su W; Yang P; Liang D; Wu L; Pan Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):272-5. PubMed ID: 24928000
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.