139 related articles for article (PubMed ID: 17036334)
1. Trigonocephaly in Muenke syndrome.
van der Meulen J; van den Ouweland A; Hoogeboom J
Am J Med Genet A; 2006 Nov; 140(22):2493-4. PubMed ID: 17036334
[TBL] [Abstract][Full Text] [Related]
2. Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene.
Graham JM; Braddock SR; Mortier GR; Lachman R; Van Dop C; Jabs EW
Am J Med Genet; 1998 May; 77(4):322-9. PubMed ID: 9600744
[TBL] [Abstract][Full Text] [Related]
3. Craniofacial morphology in Muenke syndrome.
Keller MK; Hermann NV; Darvann TA; Larsen P; Hove HD; Christensen L; Schwartz M; Marsh JL; Kreiborg S
J Craniofac Surg; 2007 Mar; 18(2):374-86. PubMed ID: 17414289
[TBL] [Abstract][Full Text] [Related]
4. [Typical features of craniofacial growth of the FGFR3-associated coronal synostosis syndrome (so-called Muenke craniosynostosis)].
Reinhart E; Eulert S; Bill J; Würzler K; Phan The L; Reuther J
Mund Kiefer Gesichtschir; 2003 May; 7(3):132-7. PubMed ID: 12764678
[TBL] [Abstract][Full Text] [Related]
5. Syndromic Craniosynostosis.
Sawh-Martinez R; Steinbacher DM
Clin Plast Surg; 2019 Apr; 46(2):141-155. PubMed ID: 30851747
[TBL] [Abstract][Full Text] [Related]
6. 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; 14(1):39-48. PubMed ID: 16251895
[TBL] [Abstract][Full Text] [Related]
7. Clinical characteristics of patients with unicoronal synostosis and mutations of fibroblast growth factor receptor 3: a preliminary report.
Cassileth LB; Bartlett SP; Glat PM; Gripp KW; Muenke M; Zackai EH; Whitaker LA
Plast Reconstr Surg; 2001 Dec; 108(7):1849-54. PubMed ID: 11743367
[TBL] [Abstract][Full Text] [Related]
8. Additional phenotypic features of Muenke syndrome in 2 Dutch families.
de Jong T; Mathijssen IM; Hoogeboom AJ
J Craniofac Surg; 2011 Mar; 22(2):571-5. PubMed ID: 21403557
[TBL] [Abstract][Full Text] [Related]
9. Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.
Assadsangabi R; Hajmomenian M; Bilaniuk LT; Vossough A
Childs Nerv Syst; 2015 May; 31(5):735-41. PubMed ID: 25686894
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic variability in Muenke syndrome-observations from five Danish families.
Öwall L; Kreiborg S; Dunø M; Hermann NV; Darvann TA; Hove H
Clin Dysmorphol; 2020 Jan; 29(1):1-9. PubMed ID: 31609728
[TBL] [Abstract][Full Text] [Related]
11. Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism.
Agochukwu NB; Solomon BD; Benson LJ; Muenke M
Am J Med Genet A; 2013 Mar; 161A(3):453-60. PubMed ID: 23378035
[TBL] [Abstract][Full Text] [Related]
12. A familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation--case report and review of the literature.
Aravidis C; Konialis CP; Pangalos CG; Kosmaidou Z
J Matern Fetal Neonatal Med; 2014 Sep; 27(14):1502-6. PubMed ID: 24168007
[TBL] [Abstract][Full Text] [Related]
13. Muenke syndrome: An international multicenter natural history study.
Kruszka P; Addissie YA; Yarnell CM; Hadley DW; Guillen Sacoto MJ; Platte P; Paelecke Y; Collmann H; Snow N; Schweitzer T; Boyadjiev SA; Aravidis C; Hall SE; Mulliken JB; Roscioli T; Muenke M
Am J Med Genet A; 2016 Apr; 170A(4):918-29. PubMed ID: 26740388
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis.
González-Del Angel A; Estandía-Ortega B; Alcántara-Ortigoza MA; Martínez-Cruz V; Gutiérrez-Tinajero DJ; Rasmussen A; Gómez-González CS
Am J Med Genet A; 2016 Dec; 170(12):3189-3196. PubMed ID: 27568649
[TBL] [Abstract][Full Text] [Related]
16. Phenotype profile of a genetic mouse model for Muenke syndrome.
Nah HD; Koyama E; Agochukwu NB; Bartlett SP; Muenke M
Childs Nerv Syst; 2012 Sep; 28(9):1483-93. PubMed ID: 22872265
[TBL] [Abstract][Full Text] [Related]
17. A Korean family with the Muenke syndrome.
Yu JE; Park DH; Yoon SH
J Korean Med Sci; 2010 Jul; 25(7):1086-9. PubMed ID: 20592905
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
Lowry RB; Jabs EW; Graham GE; Gerritsen J; Fleming J
Am J Med Genet; 2001 Nov; 104(2):112-9. PubMed ID: 11746040
[TBL] [Abstract][Full Text] [Related]
20. Molecular and cellular bases of syndromic craniosynostoses.
Bonaventure J; El Ghouzzi V
Expert Rev Mol Med; 2003 Jan; 5(4):1-17. PubMed ID: 14987407
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]