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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

189 related items for PubMed ID: 17437280

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer.
    Bergman A, Sahlin P, Emanuelsson M, Carén H, Tarnow P, Martinsson T, Grönberg H, Stenman G.
    Scand J Plast Reconstr Surg Hand Surg; 2009; 43(5):251-5. PubMed ID: 19863427
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Saethre-Chotzen syndrome: a case report.
    Peña WA, Slavotinek A, Oberoi S.
    Cleft Palate Craniofac J; 2010 May; 47(3):318-21. PubMed ID: 19860490
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Germline mutation in the FGFR3 gene in a TWIST1-negative family with Saethre-Chotzen syndrome and breast cancer.
    Sahlin P, Tarnow P, Martinsson T, Stenman G.
    Genes Chromosomes Cancer; 2009 Mar; 48(3):285-8. PubMed ID: 19025794
    [No Abstract] [Full Text] [Related]

  • 7. The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndrome.
    Foo R, Guo Y, McDonald-McGinn DM, Zackai EH, Whitaker LA, Bartlett SP.
    Plast Reconstr Surg; 2009 Dec; 124(6):2085-2095. PubMed ID: 19952666
    [Abstract] [Full Text] [Related]

  • 8. Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.
    Howard TD, Paznekas WA, Green ED, Chiang LC, Ma N, Ortiz de Luna RI, Garcia Delgado C, Gonzalez-Ramos M, Kline AD, Jabs EW.
    Nat Genet; 1997 Jan; 15(1):36-41. PubMed ID: 8988166
    [Abstract] [Full Text] [Related]

  • 9. Genetic analysis of patients with the Saethre-Chotzen phenotype.
    Chun K, Teebi AS, Jung JH, Kennedy S, Laframboise R, Meschino WS, Nakabayashi K, Scherer SW, Ray PN, Teshima I.
    Am J Med Genet; 2002 Jun 15; 110(2):136-43. PubMed ID: 12116251
    [Abstract] [Full Text] [Related]

  • 10. Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
    Woods RH, Ul-Haq E, Wilkie AOM, Jayamohan J, Richards PG, Johnson D, Lester T, Wall SA.
    Plast Reconstr Surg; 2009 Jun 15; 123(6):1801-1810. PubMed ID: 19483581
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre-Chotzen syndrome.
    Spaggiari E, Aboura A, Sinico M, Mabboux P, Dupont C, Delezoide AL, Guimiot F.
    Eur J Med Genet; 2012 Jun 15; 55(8-9):498-501. PubMed ID: 22569119
    [Abstract] [Full Text] [Related]

  • 12. Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.
    de Heer IM, de Klein A, van den Ouweland AM, Vermeij-Keers C, Wouters CH, Vaandrager JM, Hovius SE, Hoogeboom JM.
    Plast Reconstr Surg; 2005 Jun 15; 115(7):1894-902; discussion 1903-5. PubMed ID: 15923834
    [Abstract] [Full Text] [Related]

  • 13. Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome.
    Carver EA, Oram KF, Gridley T.
    Anat Rec; 2002 Oct 01; 268(2):90-2. PubMed ID: 12221714
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities.
    Firulli BA, Krawchuk D, Centonze VE, Vargesson N, Virshup DM, Conway SJ, Cserjesi P, Laufer E, Firulli AB.
    Nat Genet; 2005 Apr 01; 37(4):373-81. PubMed ID: 15735646
    [Abstract] [Full Text] [Related]

  • 16. Mutations in the human TWIST gene.
    Gripp KW, Zackai EH, Stolle CA.
    Hum Mutat; 2000 Apr 01; 15(2):150-5. PubMed ID: 10649491
    [Abstract] [Full Text] [Related]

  • 17. Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome.
    El Ghouzzi V, Lajeunie E, Le Merrer M, Cormier-Daire V, Renier D, Munnich A, Bonaventure J.
    Eur J Hum Genet; 1999 Jan 01; 7(1):27-33. PubMed ID: 10094188
    [Abstract] [Full Text] [Related]

  • 18. [Saethre-Chotzen syndrome: a case report].
    Díez de Los Ríos Quintanero B, Gracia Rojas E, Ortiz Movilla R, Cabrejas Núñez MJ, Marín Gabriel MÁ.
    Arch Argent Pediatr; 2021 Apr 01; 119(2):e129-e132. PubMed ID: 33749202
    [Abstract] [Full Text] [Related]

  • 19. Saethre–Chotzen syndrome with an atypical phenotype: identification of TWIST microdeletion by array CGH.
    Cho E, Yang TH, Shin ES, Byeon JH, Kim GH, Eun BL.
    Childs Nerv Syst; 2013 Nov 01; 29(11):2101-4. PubMed ID: 23958897
    [Abstract] [Full Text] [Related]

  • 20. Mutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen Syndrome.
    Oram KF, Gridley T.
    Genetics; 2005 Jun 01; 170(2):971-4. PubMed ID: 15802514
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.