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2. Velopharyngoplasty for noncleft velopharyngeal insufficiency: results in relation to 22q11 microdeletion. Rouillon I, Leboulanger N, Roger G, Maulet M, Marlin S, Loundon N, Portnoï MF, Denoyelle F, Garabédian EN. Arch Otolaryngol Head Neck Surg; 2009 Jul; 135(7):652-6. PubMed ID: 19620585 [Abstract] [Full Text] [Related]
9. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region. Lindsay EA, Greenberg F, Shaffer LG, Shapira SK, Scambler PJ, Baldini A. Am J Med Genet; 1995 Mar 27; 56(2):191-7. PubMed ID: 7625444 [Abstract] [Full Text] [Related]
10. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2. Matsuoka R, Takao A, Kimura M, Imamura S, Kondo C, Joh-o K, Ikeda K, Nishibatake M, Ando M, Momma K. Am J Med Genet; 1994 Nov 15; 53(3):285-9. PubMed ID: 7856665 [Abstract] [Full Text] [Related]
11. Chromosome 22q11 deletions in patients with selected outflow tract malformations. Frohn-Mulder IM, Wesby Swaay E, Bouwhuis C, Van Hemel JO, Gerritsma E, Niermeyer MF, Hess J. Genet Couns; 1999 Nov 15; 10(1):35-41. PubMed ID: 10191427 [Abstract] [Full Text] [Related]
12. [Frequency of 22q11 deletions in children with isolated conotruncal defects]. Shen L, Xu YJ, Zhao PJ, Sun K. Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jan 15; 11(1):25-8. PubMed ID: 19149917 [Abstract] [Full Text] [Related]
17. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects. Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR. J Formos Med Assoc; 1997 Jun 15; 96(6):419-23. PubMed ID: 9216164 [Abstract] [Full Text] [Related]