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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1865 1
1927 1
1928 1
1939 1
1950 1
1961 1
1977 1
1979 1
1981 1
1983 1
1984 3
1985 2
1986 6
1987 5
1988 4
1989 3
1990 7
1991 7
1992 2
1993 11
1994 6
1995 8
1996 16
1997 23
1998 25
1999 22
2000 17
2001 20
2002 23
2003 27
2004 15
2005 43
2006 21
2007 25
2008 30
2009 24
2010 25
2011 20
2012 21
2013 28
2014 32
2015 30
2016 36
2017 38
2018 35
2019 34
2020 57
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Article type
Publication date

Similar Articles for PMID: 19403480

696 results
Results by year
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Page 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. Jyonouchi S, et al. Pediatrics. 2009 May;123(5):e871-7. doi: 10.1542/peds.2008-3400. Pediatrics. 2009. PMID: 19403480 Free PMC article.
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. Jongmans MC, et al. J Med Genet. 2006 Apr;43(4):306-14. doi: 10.1136/jmg.2005.036061. Epub 2005 Sep 9. J Med Genet. 2006. PMID: 16155193 Free PMC article.
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. Aramaki M, et al. J Pediatr. 2006 Mar;148(3):410-4. doi: 10.1016/j.jpeds.2005.10.044. J Pediatr. 2006. PMID: 16615981
CHARGE syndrome.
Blake KD, Prasad C. Blake KD, et al. Orphanet J Rare Dis. 2006 Sep 7;1:34. doi: 10.1186/1750-1172-1-34. Orphanet J Rare Dis. 2006. PMID: 16959034 Free PMC article. Review.
[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 Free article. Review. Norwegian.
[Molecular diagnosis of CHARGE syndrom].
Pedersen AM, Skovby F. Pedersen AM, et al. Ugeskr Laeger. 2007 Jan 29;169(5):402-6. Ugeskr Laeger. 2007. PMID: 17280632 Review. Danish.
Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome.
Husu E, Hove HD, Farholt S, Bille M, Tranebjærg L, Vogel I, Kreiborg S. Husu E, et al. Clin Genet. 2013 Feb;83(2):125-34. doi: 10.1111/j.1399-0004.2012.01884.x. Epub 2012 Apr 30. Clin Genet. 2013. PMID: 22462537
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. Hsu P, et al. J Allergy Clin Immunol Pract. 2016 Jan-Feb;4(1):96-103.e2. doi: 10.1016/j.jaip.2015.09.004. Epub 2015 Nov 7. J Allergy Clin Immunol Pract. 2016. PMID: 26563674
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. Lalani SR, et al. BMC Med Genet. 2005 Feb 14;6:8. doi: 10.1186/1471-2350-6-8. BMC Med Genet. 2005. PMID: 15710038 Free PMC article.
Immunological abnormalities in CHARGE syndrome.
Writzl K, Cale CM, Pierce CM, Wilson LC, Hennekam RC. Writzl K, et al. Eur J Med Genet. 2007 Sep-Oct;50(5):338-45. doi: 10.1016/j.ejmg.2007.05.002. Epub 2007 May 27. Eur J Med Genet. 2007. PMID: 17684005 Review.
696 results
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