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.
180 related articles for article (PubMed ID: 20186814)
1. Histology and synchrotron radiation-based microtomography of the inner ear in a molecularly confirmed case of CHARGE syndrome. Glueckert R; Rask-Andersen H; Sergi C; Schmutzhard J; Mueller B; Beckmann F; Rittinger O; Hoefsloot LH; Schrott-Fischer A; Janecke AR Am J Med Genet A; 2010 Mar; 152A(3):665-73. PubMed ID: 20186814 [TBL] [Abstract][Full Text] [Related]
2. Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. Zentner GE; Layman WS; Martin DM; Scacheri PC Am J Med Genet A; 2010 Mar; 152A(3):674-86. PubMed ID: 20186815 [TBL] [Abstract][Full Text] [Related]
3. Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation. Lalani SR; Safiullah AM; Fernbach SD; Harutyunyan KG; Thaller C; Peterson LE; McPherson JD; Gibbs RA; White LD; Hefner M; Davenport SL; Graham JM; Bacino CA; Glass NL; Towbin JA; Craigen WJ; Neish SR; Lin AE; Belmont JW Am J Hum Genet; 2006 Feb; 78(2):303-14. PubMed ID: 16400610 [TBL] [Abstract][Full Text] [Related]
4. Congenital aplasia of the semicircular canals. Satar B; Mukherji SK; Telian SA Otol Neurotol; 2003 May; 24(3):437-46. PubMed ID: 12806296 [TBL] [Abstract][Full Text] [Related]
5. Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndrome. Adams ME; Hurd EA; Beyer LA; Swiderski DL; Raphael Y; Martin DM J Comp Neurol; 2007 Oct; 504(5):519-32. PubMed ID: 17701983 [TBL] [Abstract][Full Text] [Related]
12. A new classification for cochleovestibular malformations. Sennaroglu L; Saatci I Laryngoscope; 2002 Dec; 112(12):2230-41. PubMed ID: 12461346 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses. Granadillo JL; Wegner DJ; Paul AJ; Willing M; Sisco K; Tedder ML; Sadikovic B; Wambach JA; Baldridge D; Cole FS; Am J Med Genet A; 2021 Feb; 185(2):544-548. PubMed ID: 33184947 [TBL] [Abstract][Full Text] [Related]
15. Radial aplasia in CHARGE syndrome: a new association. Wright EM; O'Connor R; Kerr BA Eur J Med Genet; 2009; 52(4):239-41. PubMed ID: 19375527 [TBL] [Abstract][Full Text] [Related]
17. Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes. Meisner JK; Martin DM Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):81-89. PubMed ID: 31833191 [TBL] [Abstract][Full Text] [Related]
18. 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]