12605524 24146286 27189754 22929115 12919136 12479730 11903361 11389462 21740170 19467645 10686546 29287853 12729782 10807333 11195019 27329064 12081724 29032918 18554997 16791841 11920842 17964762 16854203 11253977 24357327 19620585 14986834 2057321 - Search Results

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

1

Is isolated palatal anomaly an indication to screen for 22q11 region deletion?

Reish O, Finkelstein Y, Mesterman R, Nachmani A, Wolach B, Fejgin M, Amiel A. Reish O, et al. Cleft Palate Craniofac J. 2003 Mar;40(2):176-9. doi: 10.1597/1545-1569_2003_040_0176_iipaai_2.0.co_2. Cleft Palate Craniofac J. 2003. PMID: 12605524

2

Velopharyngeal insufficiency: high detection rate of genetic abnormalities if associated with additional features.

Ockeloen CW, Simpson J, Urquhart J, Davies J, Bowden M, Patrick K, Dore J, Clayton-Smith J. Ockeloen CW, et al. Arch Dis Child. 2014 Jan;99(1):52-7. doi: 10.1136/archdischild-2013-304484. Epub 2013 Oct 21. Arch Dis Child. 2014. PMID: 24146286

3

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.

4

Effects of oropharyngeal surgery on velopharyngeal competence.

Milczuk HA. Milczuk HA. Curr Opin Otolaryngol Head Neck Surg. 2012 Dec;20(6):522-6. doi: 10.1097/MOO.0b013e32835873cc. Curr Opin Otolaryngol Head Neck Surg. 2012. PMID: 22929115 Review.

5

No justification of routine screening for 22q11 deletions in patients with overt cleft palate.

Ruiter EM, Bongers EM, Smeets D, Kuijpers-Jagtman AM, Hamel BC. Ruiter EM, et al. Clin Genet. 2003 Sep;64(3):216-9. doi: 10.1034/j.1399-0004.2003.00134.x. Clin Genet. 2003. PMID: 12919136

6

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

7

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.

8

Genetics of craniofacial development and malformation.

Wilkie AO, Morriss-Kay GM. Wilkie AO, et al. Nat Rev Genet. 2001 Jun;2(6):458-68. doi: 10.1038/35076601. Nat Rev Genet. 2001. PMID: 11389462 Review.

9

Velopharyngeal dysfunction and 22q11.2 deletion syndrome: a longitudinal study of functional outcome and preoperative prognostic factors.

Spruijt NE, Widdershoven JC, Breugem CC, Speleman L, Homveld IL, Kon M, Mink van der Molen AB. Spruijt NE, et al. Cleft Palate Craniofac J. 2012 Jul;49(4):447-55. doi: 10.1597/10-049. Epub 2011 Jul 8. Cleft Palate Craniofac J. 2012. PMID: 21740170

10

[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.

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