Similar articles for PMID: 11241468

Year	Number of Results
1981	1
1984	1
1985	1
1986	2
1987	5
1988	4
1989	3
1990	5
1991	5
1992	2
1993	3
1994	4
1995	2
1996	2
1997	6
1998	5
1999	5
2000	7
2001	4
2002	5
2003	8
2004	3
2005	13
2006	6
2007	5
2008	8
2009	7
2010	3
2011	2
2012	1
2013	3
2015	2
2016	2
2017	4
2018	1
2019	2
2020	3
2021	3
2022	2
2023	1
2024	1

1

CHARGE association with choanal atresia and inner ear hypoplasia in a child with a de novo chromosome translocation t(2;7)(p14;q21.11).

Martin DM, Sheldon S, Gorski JL. Martin DM, et al. Am J Med Genet. 2001 Mar 1;99(2):115-9. doi: 10.1002/1096-8628(2000)9999:999<00::aid-ajmg1126>3.0.co;2-8. Am J Med Genet. 2001. PMID: 11241468 Free article.

2

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. Jyonouchi S, et al. Pediatrics. 2009 May;123(5):e871-7. doi: 10.1542/peds.2008-3400. Pediatrics. 2009. PMID: 19403480 Free PMC article.

3

A CGH study of 27 patients with CHARGE association.

Sanlaville D, Romana SP, Lapierre JM, Amiel J, Genevieve D, Ozilou C, Le Lorch M, Brisset S, Gosset P, Baumann C, Turleau C, Lyonnet S, Vekemans M. Sanlaville D, et al. Clin Genet. 2002 Feb;61(2):135-8. doi: 10.1034/j.1399-0004.2002.610208.x. Clin Genet. 2002. PMID: 11940088

4

Balanced t(6;8)(6p8p;6q8q) and the CHARGE association.

Hurst JA, Meinecke P, Baraitser M. Hurst JA, et al. J Med Genet. 1991 Jan;28(1):54-5. doi: 10.1136/jmg.28.1.54. J Med Genet. 1991. PMID: 1999835 Free PMC article.

5

A patient with interstitial deletion of the short arm of chromosome 3 (pter-->p21.2::p12-->qter) and a CHARGE-like phenotype.

Wieczorek D, Bolt J, Schwechheimer K, Gillessen-Kaesbach G. Wieczorek D, et al. Am J Med Genet. 1997 Apr 14;69(4):413-7. doi: 10.1002/(sici)1096-8628(19970414)69:4<413::aid-ajmg15>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9098493

6

Trisomy 18 in a patient with CHARGE association.

Lee WT, Hou JW, Yau KI, Wang TR. Lee WT, et al. J Formos Med Assoc. 1995 Jan-Feb;94(1-2):60-2. J Formos Med Assoc. 1995. PMID: 7613237

7

Absent semicircular canals in CHARGE syndrome: radiologic spectrum of findings.

Morimoto AK, Wiggins RH 3rd, Hudgins PA, Hedlund GL, Hamilton B, Mukherji SK, Telian SA, Harnsberger HR. Morimoto AK, et al. AJNR Am J Neuroradiol. 2006 Sep;27(8):1663-71. AJNR Am J Neuroradiol. 2006. PMID: 16971610 Free PMC article.

8

CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping.

Lev D, Nakar O, Bar-Am I, Zudik A, Watemberg N, Finkelstien S, Katzin N, Lerman-Sagie T. Lev D, et al. J Med Genet. 2000 Dec;37(12):E47. doi: 10.1136/jmg.37.12.e47. J Med Genet. 2000. PMID: 11106365 Free PMC article. No abstract available.

9

Choanal atresia and associated anomalies: the CHARGE association.

Duncan NO 3rd, Miller RH, Catlin FI. Duncan NO 3rd, et al. Int J Pediatr Otorhinolaryngol. 1988 May;15(2):129-35. doi: 10.1016/0165-5876(88)90063-8. Int J Pediatr Otorhinolaryngol. 1988. PMID: 3397231

10

SEMA3E mutation in a patient with CHARGE syndrome.

Lalani SR, Safiullah AM, Molinari LM, Fernbach SD, Martin DM, Belmont JW. Lalani SR, et al. J Med Genet. 2004 Jul;41(7):e94. doi: 10.1136/jmg.2003.017640. J Med Genet. 2004. PMID: 15235037 Free PMC article. No abstract available.

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