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

Year Number of Results
2006 1
2007 2
2008 9
2009 7
2010 5
2011 3
2012 4
2013 4
2014 2
2015 4
2016 1
2017 1
2018 6
2019 6
2020 1
2021 1
2023 1
2024 1

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53 results

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Page 1
Molecular genetics of 22q11.2 deletion syndrome.
Morrow BE, McDonald-McGinn DM, Emanuel BS, Vermeesch JR, Scambler PJ. Morrow BE, et al. Am J Med Genet A. 2018 Oct;176(10):2070-2081. doi: 10.1002/ajmg.a.40504. Am J Med Genet A. 2018. PMID: 30380194 Free PMC article. Review.
Velo-Cardio-Facial Syndrome.
Gothelf D, Frisch A, Michaelovsky E, Weizman A, Shprintzen RJ. Gothelf D, et al. J Ment Health Res Intellect Disabil. 2009 Apr;2(2):149-167. doi: 10.1080/19315860902756136. J Ment Health Res Intellect Disabil. 2009. PMID: 20111667 Free PMC article.
Velopharyngeal insufficiency: diagnosis and management.
Shprintzen RJ, Marrinan E. Shprintzen RJ, et al. Curr Opin Otolaryngol Head Neck Surg. 2009 Aug;17(4):302-7. doi: 10.1097/MOO.0b013e32832cbd6b. Curr Opin Otolaryngol Head Neck Surg. 2009. PMID: 19448542 Free PMC article. Review.
Velo-cardio-facial syndrome: 30 Years of study.
Shprintzen RJ. Shprintzen RJ. Dev Disabil Res Rev. 2008;14(1):3-10. doi: 10.1002/ddrr.2. Dev Disabil Res Rev. 2008. PMID: 18636631 Free PMC article. Review.
22q and two: 22q11.2 deletion syndrome and coexisting conditions.
Cohen JL, Crowley TB, McGinn DE, McDougall C, Unolt M, Lambert MP, Emanuel BS, Zackai EH, McDonald-McGinn DM. Cohen JL, et al. Am J Med Genet A. 2018 Oct;176(10):2203-2214. doi: 10.1002/ajmg.a.40494. Epub 2018 Sep 23. Am J Med Genet A. 2018. PMID: 30244528 Free PMC article.
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, Pontillo M, Armando M, Di Fabio F, Vicari S, van den Bree M, Moss H, Owen MJ, Murphy KC, Murphy CM, Murphy D, Schoch K, Shashi V, Tassone F, Simon TJ, Shprintzen RJ, Campbell L, Philip N, Heine-Suñer D, García-Miñaúr S, Fernández L; International 22q11.2 Brain and Behavior Consortium; Bearden CE, Vingerhoets C, van Amelsvoort T, Eliez S, Schneider M, Vorstman JAS, Gothelf D, Zackai E, Agopian AJ, Gur RE, Bassett AS, Emanuel BS, Goldmuntz E, Mitchell LE, Wang T, Morrow BE. Zhao Y, et al. Am J Hum Genet. 2020 Jan 2;106(1):26-40. doi: 10.1016/j.ajhg.2019.11.010. Epub 2019 Dec 20. Am J Hum Genet. 2020. PMID: 31870554 Free PMC article.
Pilot study on schizophrenia in Sardinia.
Ott J, Macciardi F, Shen Y, Carta MG, Murru A, Triunfo R, Robledo R, Rinaldi A, Contu L, Siniscalco M. Ott J, et al. Hum Hered. 2010;70(2):92-6. doi: 10.1159/000313844. Epub 2010 Jun 17. Hum Hered. 2010. PMID: 20558996 Free PMC article.
53 results