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CHARGE syndrome.

Blake KD, Prasad C.

Orphanet J Rare Dis. 2006 Sep 7;1:34. Review.PMID: 16959034 [PubMed - indexed for MEDLINE]Related articlesFree article

CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features.

Jyonouchi S, McDonald-McGinn DM, Bale S, Zackai EH, Sullivan KE.

Pediatrics. 2009 May;123(5):e871-7.PMID: 19403480 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2005 Dec 29.PMID: 16400610 [PubMed - indexed for MEDLINE]Related articlesFree article

CHARGE syndrome: 2005.

Carey JC.

Am J Med Genet A. 2005 Mar 15;133A(3):227. No abstract available. PMID: 15633196 [PubMed - indexed for MEDLINE]Related articles

[Molecular diagnosis of CHARGE syndrom]

Pedersen AM, Skovby F.

Ugeskr Laeger. 2007 Jan 29;169(5):402-6. Review. Danish. PMID: 17280632 [PubMed - indexed for MEDLINE]Related articles

[The CHARGE syndrome]

Klingenberg C, Andersen WH.

Tidsskr Nor Laegeforen. 2008 Jun 12;128(12):1401-5. Review. Norwegian. PMID: 18552902 [PubMed - indexed for MEDLINE]Related articlesFree article

Speculations on the pathogenesis of CHARGE syndrome.

Williams MS.

Am J Med Genet A. 2005 Mar 15;133A(3):318-25.PMID: 15637730 [PubMed - indexed for MEDLINE]Related articles

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.

Aramaki M, Udaka T, Kosaki R, Makita Y, Okamoto N, Yoshihashi H, Oki H, Nanao K, Moriyama N, Oku S, Hasegawa T, Takahashi T, Fukushima Y, Kawame H, Kosaki K.

J Pediatr. 2006 Mar;148(3):410-4.PMID: 16615981 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2005 Sep 9.PMID: 16155193 [PubMed - indexed for MEDLINE]Related articlesFree article

CHARGE association in Sweden: malformations and functional deficits.

Strömland K, Sjögreen L, Johansson M, Ekman Joelsson BM, Miller M, Danielsson S, Billstedt E, Gillberg C, Jacobsson C, Norinder JA, Granström G.

Am J Med Genet A. 2005 Mar 15;133A(3):331-9.PMID: 15633180 [PubMed - indexed for MEDLINE]Related articles

An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study.

Issekutz KA, Graham JM Jr, Prasad C, Smith IM, Blake KD.

Am J Med Genet A. 2005 Mar 15;133A(3):309-17.PMID: 15637722 [PubMed - indexed for MEDLINE]Related articles

Congenital aplasia of the semicircular canals.

Satar B, Mukherji SK, Telian SA.

Otol Neurotol. 2003 May;24(3):437-46.PMID: 12806296 [PubMed - indexed for MEDLINE]Related articles

Coloboma and other ophthalmologic anomalies in Kabuki syndrome: distinction from charge association.

Ming JE, Russell KL, Bason L, McDonald-McGinn DM, Zackai EH.

Am J Med Genet A. 2003 Dec 15;123A(3):249-52. Review.PMID: 14608645 [PubMed - indexed for MEDLINE]Related articles

Scoliosis in CHARGE: a prospective survey and two case reports.

Doyle C, Blake K.

Am J Med Genet A. 2005 Mar 15;133A(3):340-3.PMID: 15688383 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2004 Aug 8.PMID: 15300250 [PubMed - indexed for MEDLINE]Related articles

CHARGE syndrome from birth to adulthood: an individual reported on from 0 to 33 years.

Searle LC, Graham JM Jr, Prasad C, Blake KD.

Am J Med Genet A. 2005 Mar 15;133A(3):344-9.PMID: 15637714 [PubMed - indexed for MEDLINE]Related articles

Behavioral features of CHARGE syndrome (Hall-Hittner syndrome) comparison with Down syndrome, Prader-Willi syndrome, and Williams syndrome.

Graham JM Jr, Rosner B, Dykens E, Visootsak J.

Am J Med Genet A. 2005 Mar 15;133A(3):240-7.PMID: 15637708 [PubMed - indexed for MEDLINE]Related articles

Choanal atresia and associated anomalies: the CHARGE association.

Duncan NO 3rd, Miller RH, Catlin FI.

Int J Pediatr Otorhinolaryngol. 1988 May;15(2):129-35.PMID: 3397231 [PubMed - indexed for MEDLINE]Related articles

CHARGE syndrome: report of 47 cases and review.

Tellier AL, Cormier-Daire V, Abadie V, Amiel J, Sigaudy S, Bonnet D, de Lonlay-Debeney P, Morrisseau-Durand MP, Hubert P, Michel JL, Jan D, Dollfus H, Baumann C, Labrune P, Lacombe D, Philip N, LeMerrer M, Briard ML, Munnich A, Lyonnet S.

Am J Med Genet. 1998 Apr 13;76(5):402-9. Review.PMID: 9556299 [PubMed - indexed for MEDLINE]Related articles

Abnormal basiocciput development in CHARGE syndrome.

Fujita K, Aida N, Asakura Y, Kurosawa K, Niwa T, Muroya K, Adachi M, Nishimura G, Inoue T.

AJNR Am J Neuroradiol. 2009 Mar;30(3):629-34. Epub 2008 Dec 26.PMID: 19112063 [PubMed - indexed for MEDLINE]Related articlesFree article