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.
258 related articles for article (PubMed ID: 18391498)
1. Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations. Passos-Bueno MR; Sertié AL; Jehee FS; Fanganiello R; Yeh E Front Oral Biol; 2008; 12():107-143. PubMed ID: 18391498 [TBL] [Abstract][Full Text] [Related]
2. Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling. Kutkowska-Kaźmierczak A; Gos M; Obersztyn E J Appl Genet; 2018 May; 59(2):133-147. PubMed ID: 29392564 [TBL] [Abstract][Full Text] [Related]
3. Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis. Ibarra-Arce A; Almaraz-Salinas M; Martínez-Rosas V; Ortiz de Zárate-Alarcón G; Flores-Peña L; Romero-Valdovinos M; Olivo-Díaz A Mol Genet Genomic Med; 2020 Aug; 8(8):e1266. PubMed ID: 32510873 [TBL] [Abstract][Full Text] [Related]
4. 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 [TBL] [Abstract][Full Text] [Related]
5. Molecular Mechanisms Involved in Craniosynostosis. Yapijakis C; Pachis N; Sotiriadou T; Vaila C; Michopoulou V; Vassiliou S In Vivo; 2023; 37(1):36-46. PubMed ID: 36593018 [TBL] [Abstract][Full Text] [Related]
6. Genetic Analysis of Syndromic and Nonsyndromic Patients With Craniosynostosis Identifies Novel Mutations in the Apostolopoulou D; Kaxira OS; Hatzaki A; Panagopoulos KP; Alexandrou K; Stratoudakis A; Kollia P; Aleporou V Cleft Palate Craniofac J; 2018 Sep; 55(8):1092-1102. PubMed ID: 29561715 [TBL] [Abstract][Full Text] [Related]
7. Heterozygous mutations in ERF cause syndromic craniosynostosis with multiple suture involvement. Chaudhry A; Sabatini P; Han L; Ray PN; Forrest C; Bowdin S Am J Med Genet A; 2015 Nov; 167A(11):2544-7. PubMed ID: 26097063 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses. Ohishi A; Nishimura G; Kato F; Ono H; Maruwaka K; Ago M; Suzumura H; Hirose E; Uchida Y; Fukami M; Ogata T Am J Med Genet A; 2017 Jan; 173(1):157-162. PubMed ID: 27683237 [TBL] [Abstract][Full Text] [Related]
10. Genetic Syndromes Associated with Craniosynostosis. Ko JM J Korean Neurosurg Soc; 2016 May; 59(3):187-91. PubMed ID: 27226847 [TBL] [Abstract][Full Text] [Related]
11. Mild isolated craniosynostosis due to a novel FGFR3 mutation, p.Ala334Thr. Barroso E; Pérez-Carrizosa V; García-Recuero I; Glucksman MJ; Wilkie AO; García-Minaur S; Heath KE Am J Med Genet A; 2011 Dec; 155A(12):3050-3. PubMed ID: 22038757 [TBL] [Abstract][Full Text] [Related]
17. Roles of FGFR2 and twist in human craniosynostosis: insights from genetic mutations in cranial osteoblasts. Marie PJ; Kaabeche K; Guenou H Front Oral Biol; 2008; 12():144-159. PubMed ID: 18391499 [TBL] [Abstract][Full Text] [Related]
18. Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses. Agochukwu NB; Solomon BD; Muenke M Childs Nerv Syst; 2012 Sep; 28(9):1447-63. PubMed ID: 22872262 [TBL] [Abstract][Full Text] [Related]
19. Genetic basis of potential therapeutic strategies for craniosynostosis. Melville H; Wang Y; Taub PJ; Jabs EW Am J Med Genet A; 2010 Dec; 152A(12):3007-15. PubMed ID: 21082653 [TBL] [Abstract][Full Text] [Related]