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

Year Number of Results
2000 2
2001 3
2002 4
2003 4
2006 2
2007 1
2008 2
2009 2
2010 1
2011 1
2012 2
2013 2
2014 2
2015 1
2016 1
2017 3
2018 2
2022 0
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28 results
Results by year
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Page 1
22q11.2 deletion syndrome.
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. McDonald-McGinn DM, et al. Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Nat Rev Dis Primers. 2015. PMID: 27189754 Free PMC article. Review.
Otolaryngologic manifestations of the 22q11.2 deletion syndrome.
Dyce O, McDonald-McGinn D, Kirschner RE, Zackai E, Young K, Jacobs IN. Dyce O, et al. Arch Otolaryngol Head Neck Surg. 2002 Dec;128(12):1408-12. doi: 10.1001/archotol.128.12.1408. Arch Otolaryngol Head Neck Surg. 2002. PMID: 12479730
Autosomal dominant isolated velopharyngeal insufficiency.
Vantrappen G, Rommel N, Wellens W, Cremers CW, Fryns JP, Devriendt K. Vantrappen G, et al. Clin Genet. 2002 Jan;61(1):74-6. doi: 10.1034/j.1399-0004.2002.610115.x. Clin Genet. 2002. PMID: 11903361 No abstract available.
[Velopharyngeal insufficiency in children].
Rouillon I, Leboulanger N, Roger G, Marlin S, Garabédian EN. Rouillon I, et al. Ann Otolaryngol Chir Cervicofac. 2009 Jun;126(3):155-61. doi: 10.1016/j.aorl.2009.03.006. Epub 2009 May 20. Ann Otolaryngol Chir Cervicofac. 2009. PMID: 19467645 Review. French. No abstract available.
28 results