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Journal Abstract Search

284 related items for PubMed ID: 32822871

  • 1. Early mandibular morphological differences in patients with FGFR2 and FGFR3-related syndromic craniosynostoses: A 3D comparative study.
    Morice A, Cornette R, Giudice A, Collet C, Paternoster G, Arnaud É, Galliani E, Picard A, Legeai-Mallet L, Khonsari RH.
    Bone; 2020 Dec; 141():115600. PubMed ID: 32822871
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  • 4. Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis.
    Hoshino Y, Takechi M, Moazen M, Steacy M, Koyabu D, Furutera T, Ninomiya Y, Nuri T, Pauws E, Iseki S.
    J Anat; 2023 Mar; 242(3):387-401. PubMed ID: 36394990
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  • 7. Mandibular asymmetry in patients with the crouzon or apert syndrome.
    Elmi P, Reitsma JH, Buschang PH, Wolvius EB, Ongkosuwito EM.
    Cleft Palate Craniofac J; 2015 May; 52(3):327-35. PubMed ID: 24878346
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  • 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
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  • 14. Severe craniolacunae and upper and lower extremity anomalies resulting from Crouzon syndrome, FGFR2 mutation, and Ser347Cys variant.
    Raposo-Amaral CE, Oliveira YM, Denadai R, Raposo-Amaral CA, Ghizoni E.
    Childs Nerv Syst; 2021 Jul; 37(7):2391-2397. PubMed ID: 33404724
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  • 17. Syndromic craniosynostosis: from history to hydrogen bonds.
    Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV.
    Orthod Craniofac Res; 2007 May; 10(2):67-81. PubMed ID: 17552943
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  • 18. Sequence analysis of fibroblast growth factor receptor 2 ( FGFR2 ) in Japanese patients with craniosynostosis.
    Sakai N, Tokunaga K, Yamazaki Y, Shida H, Sakata Y, Susami T, Nakakita N, Takato T, Uchinuma E.
    J Craniofac Surg; 2001 Nov; 12(6):580-5. PubMed ID: 11711827
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  • 19. Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.
    Heuzé Y, Martínez-Abadías N, Stella JM, Arnaud E, Collet C, García Fructuoso G, Alamar M, Lo LJ, Boyadjiev SA, Di Rocco F, Richtsmeier JT.
    Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):250-9. PubMed ID: 24578066
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