Expanding the "E" in CHARGE - PubMed (original) (raw)
Case Reports
. 2008 Jul 15;146A(14):1890-2.
doi: 10.1002/ajmg.a.32376.
Affiliations
- PMID: 18553515
- DOI: 10.1002/ajmg.a.32376
Case Reports
Expanding the "E" in CHARGE
Anas M Alazami et al. Am J Med Genet A. 2008.
No abstract available
Similar articles
- Gene symbol: CHD7. Disease: CHARGE syndrome.
Ellison J. Ellison J. Hum Genet. 2008 Oct;124(3):323. Hum Genet. 2008. PMID: 18846688 No abstract available. - [CHARGE syndrome].
Matsumoto T, Miyahara H, Morifuji K, Sasaki N. Matsumoto T, et al. Nihon Rinsho. 2006 Sep 28;Suppl 3:453-6. Nihon Rinsho. 2006. PMID: 17022586 Review. Japanese. No abstract available. - 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. Vissers LE, et al. Nat Genet. 2004 Sep;36(9):955-7. doi: 10.1038/ng1407. Epub 2004 Aug 8. Nat Genet. 2004. PMID: 15300250 - ["CHARGE" association].
Barak A, Gabis L, Mogilner B, Gelman-Kohan S. Barak A, et al. Harefuah. 1997 Feb 16;132(4):254-8, 311. Harefuah. 1997. PMID: 9153893 Hebrew. - [The CHARGE syndrome].
Klingenberg C, Andersen WH. Klingenberg C, et al. Tidsskr Nor Laegeforen. 2008 Jun 12;128(12):1401-5. Tidsskr Nor Laegeforen. 2008. PMID: 18552902 Review. Norwegian.
Cited by
- Deformity Reconstruction Surgery for Tibial Hemimelia.
Chong DY, Paley D. Chong DY, et al. Children (Basel). 2021 May 31;8(6):461. doi: 10.3390/children8060461. Children (Basel). 2021. PMID: 34072809 Free PMC article. Review. - Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes.
George A, Cogliati T, Brooks BP. George A, et al. Exp Eye Res. 2020 Apr;193:107940. doi: 10.1016/j.exer.2020.107940. Epub 2020 Feb 4. Exp Eye Res. 2020. PMID: 32032630 Free PMC article. Review. - Tibial hemimelia: new classification and reconstructive options.
Paley D. Paley D. J Child Orthop. 2016 Dec;10(6):529-555. doi: 10.1007/s11832-016-0785-x. Epub 2016 Dec 1. J Child Orthop. 2016. PMID: 27909860 Free PMC article. Review. - Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria.
Hale CL, Niederriter AN, Green GE, Martin DM. Hale CL, et al. Am J Med Genet A. 2016 Feb;170A(2):344-354. doi: 10.1002/ajmg.a.37435. Epub 2015 Nov 21. Am J Med Genet A. 2016. PMID: 26590800 Free PMC article. - Unique phenotype in a patient with CHARGE syndrome.
Jain S, Kim HG, Lacbawan F, Meliciani I, Wenzel W, Kurth I, Sharma J, Schoeneman M, Ten S, Layman LC, Jacobson-Dickman E. Jain S, et al. Int J Pediatr Endocrinol. 2011 Oct 13;2011(1):11. doi: 10.1186/1687-9856-2011-11. Int J Pediatr Endocrinol. 2011. PMID: 21995344 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources