450 related articles for article (PubMed ID: 19403480)
1. 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. PubMed ID: 19403480
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 16615981
[TBL] [Abstract][Full Text] [Related]
3. 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. CHARGE syndrome.
Blake KD; Prasad C
Orphanet J Rare Dis; 2006 Sep; 1():34. PubMed ID: 16959034
[TBL] [Abstract][Full Text] [Related]
5. [The CHARGE syndrome].
Klingenberg C; Andersen WH
Tidsskr Nor Laegeforen; 2008 Jun; 128(12):1401-5. PubMed ID: 18552902
[TBL] [Abstract][Full Text] [Related]
6. [Molecular diagnosis of CHARGE syndrom].
Pedersen AM; Skovby F
Ugeskr Laeger; 2007 Jan; 169(5):402-6. PubMed ID: 17280632
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. The Immune Phenotype of Patients with CHARGE Syndrome.
Hsu P; Ma A; Barnes EH; Wilson M; Hoefsloot LH; Rinne T; Munns C; Williams G; Wong M; Mehr S
J Allergy Clin Immunol Pract; 2016; 4(1):96-103.e2. PubMed ID: 26563674
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. SNP genotyping to screen for a common deletion in CHARGE syndrome.
Lalani SR; Safiullah AM; Fernbach SD; Phillips M; Bacino CA; Molinari LM; Glass NL; Towbin JA; Craigen WJ; Belmont JW
BMC Med Genet; 2005 Feb; 6():8. PubMed ID: 15710038
[TBL] [Abstract][Full Text] [Related]
13. [The CHARGE association].
Finel E; Parent P; Giroux JD; de Parscau L
Arch Pediatr; 1996 Oct; 3(10):1020-5. PubMed ID: 8952799
[TBL] [Abstract][Full Text] [Related]
14. CHARGE syndrome in nine patients from China.
Cheng SSW; Luk HM; Chan DKH; Lo IFM
Am J Med Genet A; 2020 Jan; 182(1):15-19. PubMed ID: 31729160
[TBL] [Abstract][Full Text] [Related]
15. Immunological abnormalities in CHARGE syndrome.
Writzl K; Cale CM; Pierce CM; Wilson LC; Hennekam RC
Eur J Med Genet; 2007; 50(5):338-45. PubMed ID: 17684005
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated.
Corsten-Janssen N; Saitta SC; Hoefsloot LH; McDonald-McGinn DM; Driscoll DA; Derks R; Dickinson KA; Kerstjens-Frederikse WS; Emanuel BS; Zackai EH; van Ravenswaaij-Arts CM
Mol Syndromol; 2013 Jun; 4(5):235-45. PubMed ID: 23885230
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome.
Wincent J; Holmberg E; Strömland K; Soller M; Mirzaei L; Djureinovic T; Robinson K; Anderlid B; Schoumans J
Clin Genet; 2008 Jul; 74(1):31-8. PubMed ID: 18445044
[TBL] [Abstract][Full Text] [Related]
20. The spectrum of clinical features in CHARGE syndrome.
Davenport SL; Hefner MA; Mitchell JA
Clin Genet; 1986 Apr; 29(4):298-310. PubMed ID: 2424647
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
