BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

255 related articles for article (PubMed ID: 18449898)

  • 1. Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
    Crétolle C; Pelet A; Sanlaville D; Zérah M; Amiel J; Jaubert F; Révillon Y; Baala L; Munnich A; Nihoul-Fékété C; Lyonnet S
    Hum Mutat; 2008 Jul; 29(7):903-10. PubMed ID: 18449898
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.
    Köchling J; Karbasiyan M; Reis A
    Eur J Hum Genet; 2001 Aug; 9(8):599-605. PubMed ID: 11528505
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ZFHX1B mutations in patients with Mowat-Wilson syndrome.
    Dastot-Le Moal F; Wilson M; Mowat D; Collot N; Niel F; Goossens M
    Hum Mutat; 2007 Apr; 28(4):313-21. PubMed ID: 17203459
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical features and HLXB9 gene mutation of a sporadic Chinese Currarino's syndrome case.
    Liang Y; Wang J; Cai W
    J Pediatr Surg; 2007 Jun; 42(6):E27-30. PubMed ID: 17560192
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HLXB9 homeobox gene and caudal regression syndrome.
    Merello E; De Marco P; Mascelli S; Raso A; Calevo MG; Torre M; Cama A; Lerone M; Martucciello G; Capra V
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):205-9. PubMed ID: 16498628
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome.
    Zu S; Winberg J; Arnberg F; Palmer G; Svensson PJ; Wester T; Nordenskjöld A
    J Pediatr Surg; 2011 Jul; 46(7):1390-5. PubMed ID: 21763840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New clinical and therapeutic perspectives in Currarino syndrome (study of 29 cases).
    Crétolle C; Zérah M; Jaubert F; Sarnacki S; Révillon Y; Lyonnet S; Nihoul-Fékété C
    J Pediatr Surg; 2006 Jan; 41(1):126-31; discussion 126-31. PubMed ID: 16410121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Currarino triad: the variable expression.
    Emans PJ; Kootstra G; Marcelis CL; Beuls EA; van Heurn LW
    J Pediatr Surg; 2005 Aug; 40(8):1238-42. PubMed ID: 16080925
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
    Merello E; De Marco P; Ravegnani M; Riccipetitoni G; Cama A; Capra V
    Eur J Med Genet; 2013 Dec; 56(12):648-54. PubMed ID: 24095820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype.
    Markljung E; Adamovic T; Cao J; Naji H; Kaiser S; Wester T; Nordenskjöld A
    Gene; 2012 Oct; 507(1):50-3. PubMed ID: 22820079
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Currarino syndrome: variable imaging features in three siblings with HLXB9 gene mutation.
    Kim AY; Yoo SY; Kim JH; Eo H; Jeon TY
    Clin Imaging; 2013; 37(2):398-402. PubMed ID: 23466002
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Currarino syndrome: variability of imaging findings in 22 molecular-genetically identified (HLXB9 mutation) patients from five families].
    Riebel T; Köchling J; Scheer I; Oellinger J; Reis A
    Rofo; 2004 Apr; 176(4):564-9. PubMed ID: 15088182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.
    Hagan DM; Ross AJ; Strachan T; Lynch SA; Ruiz-Perez V; Wang YM; Scambler P; Custard E; Reardon W; Hassan S; Nixon P; Papapetrou C; Winter RM; Edwards Y; Morrison K; Barrow M; Cordier-Alex MP; Correia P; Galvin-Parton PA; Gaskill S; Gaskin KJ; Garcia-Minaur S; Gereige R; Hayward R; Homfray T
    Am J Hum Genet; 2000 May; 66(5):1504-15. PubMed ID: 10749657
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.
    Kim IS; Oh SY; Choi SJ; Kim JH; Park KH; Park HK; Kim JW; Ki CS
    J Hum Genet; 2007; 52(8):698-701. PubMed ID: 17612791
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and mutational spectrum of Mowat-Wilson syndrome.
    Zweier C; Thiel CT; Dufke A; Crow YJ; Meinecke P; Suri M; Ala-Mello S; Beemer F; Bernasconi S; Bianchi P; Bier A; Devriendt K; Dimitrov B; Firth H; Gallagher RC; Garavelli L; Gillessen-Kaesbach G; Hudgins L; Kääriäinen H; Karstens S; Krantz I; Mannhardt A; Medne L; Mücke J; Kibaek M; Krogh LN; Peippo M; Rittinger O; Schulz S; Schelley SL; Temple IK; Dennis NR; Van der Knaap MS; Wheeler P; Yerushalmi B; Zenker M; Seidel H; Lachmeijer A; Prescott T; Kraus C; Lowry RB; Rauch A
    Eur J Med Genet; 2005; 48(2):97-111. PubMed ID: 16053902
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodynia.
    Volk A; Karbasiyan M; Semmler A; Todt U; Urbach H; Klockgether T; Linnebank M
    Birth Defects Res A Clin Mol Teratol; 2007 Mar; 79(3):249-51. PubMed ID: 17183586
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A previously unreported mutation in a Currarino syndrome kindred.
    Wang RY; Jones JR; Chen S; Rogers RC; Friez MJ; Schwartz CE; Graham JM
    Am J Med Genet A; 2006 Sep; 140(18):1923-30. PubMed ID: 16906559
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
    Ross AJ; Ruiz-Perez V; Wang Y; Hagan DM; Scherer S; Lynch SA; Lindsay S; Custard E; Belloni E; Wilson DI; Wadey R; Goodman F; Orstavik KH; Monclair T; Robson S; Reardon W; Burn J; Scambler P; Strachan T
    Nat Genet; 1998 Dec; 20(4):358-61. PubMed ID: 9843207
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.