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 *

106 related articles for article (PubMed ID: 18629881)

  • 1. Sacral appendage in a child with an FGFR2 mutation: a report and review.
    Shanske AL; Staffenberg D; Goodrich JT
    Am J Med Genet A; 2008 Aug; 146A(16):2172-5. PubMed ID: 18629881
    [No Abstract]   [Full Text] [Related]  

  • 2. A mutation in FGFR2 in a child with Pfeiffer syndrome and a sacral appendage.
    Lai AHM; Tan YM; Law HY; Yeow VKL
    Clin Dysmorphol; 2008 Jan; 17(1):73-74. PubMed ID: 18049087
    [No Abstract]   [Full Text] [Related]  

  • 3. A cloverleaf skull associated with Crouzon syndrome.
    Chen CP; Lin SP; Su YN; Huang JK; Wang W
    Arch Dis Child Fetal Neonatal Ed; 2006 Mar; 91(2):F98. PubMed ID: 16492963
    [No Abstract]   [Full Text] [Related]  

  • 4. Sacral appendage associated with a mutation in FGFR2.
    Sweeney E; Ellis I; May P
    Clin Dysmorphol; 2002 Jul; 11(3):221-2. PubMed ID: 12072807
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Atypical Crouzon syndrome with a novel Cys62Arg mutation in FGFR2 presenting with sagittal synostosis.
    Sharma VP; Wall SA; Lord H; Lester T; Wilkie AO
    Cleft Palate Craniofac J; 2012 May; 49(3):373-7. PubMed ID: 22117175
    [TBL] [Abstract][Full Text] [Related]  

  • 6. S267P mutation in FGFR2: first report in a patient with Crouzon syndrome.
    Ke R; Yang X; Ge M; Cai T; Lei J; Mu X
    J Craniofac Surg; 2015 Mar; 26(2):592-4. PubMed ID: 25759927
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
    Anderson PJ; Netherway DJ; Cox TC; Roscioli T; David DJ
    J Craniofac Surg; 2006 Jan; 17(1):166-72. PubMed ID: 16432427
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome.
    Chaisrisawadisuk S; Hammam E; Molloy CJ; Barnett C; Anderson PJ; Moore MH
    J Craniofac Surg; 2021 Jan-Feb 01; 32(1):261-264. PubMed ID: 32956303
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome.
    Fenwick AL; Goos JA; Rankin J; Lord H; Lester T; Hoogeboom AJ; van den Ouweland AM; Wall SA; Mathijssen IM; Wilkie AO
    BMC Med Genet; 2014 Aug; 15():95. PubMed ID: 25174698
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
    Nur BG; Pehlivanoğlu S; Mıhçı E; Calışkan M; Demir D; Alper OM; Kayserili H; Lüleci G
    Pediatr Neurol; 2014 May; 50(5):482-90. PubMed ID: 24656465
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lumpers, splitters, and FGFRs.
    Winter RM; Reardon W
    Am J Med Genet; 1996 Jun; 63(3):501-2. PubMed ID: 8737660
    [No Abstract]   [Full Text] [Related]  

  • 13. Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: Implications for genetic testing in "paternal age-effect" syndromes.
    Goriely A; Lord H; Lim J; Johnson D; Lester T; Firth HV; Wilkie AO
    Am J Med Genet A; 2010 Aug; 152A(8):2067-73. PubMed ID: 20635358
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
    Roscioli T; Elakis G; Cox TC; Moon DJ; Venselaar H; Turner AM; Le T; Hackett E; Haan E; Colley A; Mowat D; Worgan L; Kirk EP; Sachdev R; Thompson E; Gabbett M; McGaughran J; Gibson K; Gattas M; Freckmann ML; Dixon J; Hoefsloot L; Field M; Hackett A; Kamien B; Edwards M; Adès LC; Collins FA; Wilson MJ; Savarirayan R; Tan TY; Amor DJ; McGillivray G; White SM; Glass IA; David DJ; Anderson PJ; Gianoutsos M; Buckley MF
    Am J Med Genet C Semin Med Genet; 2013 Nov; 163C(4):259-70. PubMed ID: 24127277
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel fibroblast growth factor receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome.
    Locuratolo N; Baffico M; Baldi M; Parisi V; Micacchi F; Angelucci V; Rojas Beccaglia M; Pirro C; Fattapposta F
    Arch Ital Biol; 2011 Sep; 149(3):313-7. PubMed ID: 22028092
    [No Abstract]   [Full Text] [Related]  

  • 16. Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.
    Passos-Bueno MR; Sertié AL; Richieri-Costa A; Alonso LG; Zatz M; Alonso N; Brunoni D; Ribeiro SF
    Am J Med Genet; 1998 Jul; 78(3):237-41. PubMed ID: 9677057
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.
    Perlyn CA; DeLeon VB; Babbs C; Govier D; Burell L; Darvann T; Kreiborg S; Morriss-Kay G
    Cleft Palate Craniofac J; 2006 Nov; 43(6):740-8. PubMed ID: 17105336
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation.
    Tan AP; Mankad K
    Childs Nerv Syst; 2018 Jan; 34(1):23-25. PubMed ID: 29067506
    [No Abstract]   [Full Text] [Related]  

  • 19. FGFR2 splice site mutations in Crouzon and Pfeiffer syndromes: two novel variants.
    Apra C; Collet C; Arnaud E; Di Rocco F
    Clin Genet; 2016 Jun; 89(6):746-8. PubMed ID: 26841243
    [No Abstract]   [Full Text] [Related]  

  • 20. Fibroblast growth factor receptor 2 and its role in caudal appendage and craniosynostosis.
    Sureka D; Hudgins L
    J Craniofac Surg; 2010 Sep; 21(5):1346-9. PubMed ID: 20856019
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.