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.
195 related articles for article (PubMed ID: 19058860)
1. Postoperative airway events of individuals with CHARGE syndrome. Blake K; MacCuspie J; Hartshorne TS; Roy M; Davenport SL; Corsten G Int J Pediatr Otorhinolaryngol; 2009 Feb; 73(2):219-26. PubMed ID: 19058860 [TBL] [Abstract][Full Text] [Related]
2. CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. Jongmans MC; Admiraal RJ; van der Donk KP; Vissers LE; Baas AF; Kapusta L; van Hagen JM; Donnai D; de Ravel TJ; Veltman JA; Geurts van Kessel A; De Vries BB; Brunner HG; Hoefsloot LH; van Ravenswaaij CM J Med Genet; 2006 Apr; 43(4):306-14. PubMed ID: 16155193 [TBL] [Abstract][Full Text] [Related]
4. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Vissers LE; van Ravenswaaij CM; Admiraal R; Hurst JA; de Vries BB; Janssen IM; van der Vliet WA; Huys EH; de Jong PJ; Hamel BC; Schoenmakers EF; Brunner HG; Veltman JA; van Kessel AG Nat Genet; 2004 Sep; 36(9):955-7. PubMed ID: 15300250 [TBL] [Abstract][Full Text] [Related]
6. New recognized ophthalmic morphologic anomalies in CHARGE syndrome caused by the R2319C mutation in the CHD7 gene. Holak HM; Kohlhase J; Holak SA; Holak NH Ophthalmic Genet; 2008 Jun; 29(2):79-84. PubMed ID: 18484313 [TBL] [Abstract][Full Text] [Related]
7. Predictive factors for success after transnasal endoscopic treatment of choanal atresia. Teissier N; Kaguelidou F; Couloigner V; François M; Van Den Abbeele T Arch Otolaryngol Head Neck Surg; 2008 Jan; 134(1):57-61. PubMed ID: 18209138 [TBL] [Abstract][Full Text] [Related]
11. Characterization of congenital anomalies in individuals with choanal atresia. Burrow TA; Saal HM; de Alarcon A; Martin LJ; Cotton RT; Hopkin RJ Arch Otolaryngol Head Neck Surg; 2009 Jun; 135(6):543-7. PubMed ID: 19528400 [TBL] [Abstract][Full Text] [Related]
12. Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome. Husu E; Hove HD; Farholt S; Bille M; Tranebjærg L; Vogel I; Kreiborg S Clin Genet; 2013 Feb; 83(2):125-34. PubMed ID: 22462537 [TBL] [Abstract][Full Text] [Related]
13. Cochlear implantation in Children with CHARGE syndrome: therapeutic decisions and outcomes. Lanson BG; Green JE; Roland JT; Lalwani AK; Waltzman SB Laryngoscope; 2007 Jul; 117(7):1260-6. PubMed ID: 17507827 [TBL] [Abstract][Full Text] [Related]
14. Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development. Sanlaville D; Etchevers HC; Gonzales M; Martinovic J; Clément-Ziza M; Delezoide AL; Aubry MC; Pelet A; Chemouny S; Cruaud C; Audollent S; Esculpavit C; Goudefroye G; Ozilou C; Fredouille C; Joye N; Morichon-Delvallez N; Dumez Y; Weissenbach J; Munnich A; Amiel J; Encha-Razavi F; Lyonnet S; Vekemans M; Attié-Bitach T J Med Genet; 2006 Mar; 43(3):211-217. PubMed ID: 16169932 [TBL] [Abstract][Full Text] [Related]
15. CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome. Batsukh T; Pieper L; Koszucka AM; von Velsen N; Hoyer-Fender S; Elbracht M; Bergman JE; Hoefsloot LH; Pauli S Hum Mol Genet; 2010 Jul; 19(14):2858-66. PubMed ID: 20453063 [TBL] [Abstract][Full Text] [Related]
16. Cranial nerve abnormalities in CHARGE association. Byerly KA; Pauli RM Am J Med Genet; 1993 Mar; 45(6):751-7. PubMed ID: 8053985 [TBL] [Abstract][Full Text] [Related]