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155 related items for PubMed ID: 33749202

  • 1. [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; 119(2):e129-e132. PubMed ID: 33749202
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  • 2. 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
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  • 3. 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
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  • 5. 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 01; 115(7):1894-902; discussion 1903-5. PubMed ID: 15923834
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  • 7. Y-craniosynostosis by premature fusion of the metopic and coronal sutures: a new nosological entity or a variety of Saethre-Chotzen syndrome?
    di Rocco F, Benoit A, Vigneron J, Segura PB, Klein O, Collet C, Arnaud E.
    Birth Defects Res A Clin Mol Teratol; 2015 Apr 01; 103(4):306-10. PubMed ID: 25808521
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  • 9. Postnatal Progressive Craniosynostosis in Syndromic Conditions: Two Patients With Saethre-Chotzen Due to TWIST1 Gene Deletions and Review of the Literature.
    Alawneh RJ, Johnson AL, Hoover-Fong JE, Jackson EM, Steinberg JP, MacCarrick G.
    Cleft Palate Craniofac J; 2023 Aug 01; 60(8):1021-1028. PubMed ID: 35354337
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  • 12. 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
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  • 13. Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome.
    de Heer IM, Hoogeboom J, Vermeij-Keers C, de Klein A, Vaandrager JM.
    J Craniofac Surg; 2004 Nov 01; 15(6):1048-52. PubMed ID: 15547403
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  • 14. Combined metopic and unilateral coronal synostoses: a phenotypic conundrum.
    Sauerhammer TM, Patel K, Oh AK, Proctor MR, Mulliken JB, Rogers GF.
    J Craniofac Surg; 2014 Mar 01; 25(2):437-40. PubMed ID: 24448523
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  • 15. Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
    Sharma VP, Fenwick AL, Brockop MS, McGowan SJ, Goos JA, Hoogeboom AJ, Brady AF, Jeelani NO, Lynch SA, Mulliken JB, Murray DJ, Phipps JM, Sweeney E, Tomkins SE, Wilson LC, Bennett S, Cornall RJ, Broxholme J, Kanapin A, 500 Whole-Genome Sequences (WGS500) Consortium, Johnson D, Wall SA, van der Spek PJ, Mathijssen IM, Maxson RE, Twigg SR, Wilkie AO.
    Nat Genet; 2013 Mar 01; 45(3):304-7. PubMed ID: 23354436
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  • 16. Quantitative Morphologic Analysis of Cranial Vault in Twist1+/- Mice: Implications in Craniosynostosis.
    Nuri T, Ota M, Ueda K, Iseki S.
    Plast Reconstr Surg; 2022 Jan 01; 149(1):28e-37e. PubMed ID: 34936613
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  • 17. Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
    Kress W, Schropp C, Lieb G, Petersen B, Büsse-Ratzka M, Kunz J, Reinhart E, Schäfer WD, Sold J, Hoppe F, Pahnke J, Trusen A, Sörensen N, Krauss J, Collmann H.
    Eur J Hum Genet; 2006 Jan 01; 14(1):39-48. PubMed ID: 16251895
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  • 19. Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome.
    Teng CS, Ting MC, Farmer DT, Brockop M, Maxson RE, Crump JG.
    Elife; 2018 Oct 25; 7():. PubMed ID: 30375332
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  • 20. 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
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