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9. Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome. Saitta SC, Harris SE, McDonald-McGinn DM, Emanuel BS, Tonnesen MK, Zackai EH, Seitz SC, Driscoll DA. Am J Med Genet A; 2004 Jan 30; 124A(3):313-7. PubMed ID: 14708107 [Abstract] [Full Text] [Related]
10. 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 30; 96(6):419-23. PubMed ID: 9216164 [Abstract] [Full Text] [Related]
12. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence. McDonald-McGinn DM, Driscoll DA, Emanuel BS, Goldmuntz E, Clark BJ, Solot C, Cohen M, Schultz P, LaRossa D, Randall P, Zackai EH. Pediatrics; 1997 May 30; 99(5):E9. PubMed ID: 9113966 [Abstract] [Full Text] [Related]