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8. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome. Van Esch H; Groenen P; Fryns JP; Van de Ven W; Devriendt K Genet Couns; 1999; 10(1):59-65. PubMed ID: 10191430 [TBL] [Abstract][Full Text] [Related]
9. Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion. Van Hemel JO; Schaap C; Van Opstal D; Mulder MP; Niermeijer MF; Meijers JH J Med Genet; 1995 Aug; 32(8):657-8. PubMed ID: 7473663 [TBL] [Abstract][Full Text] [Related]
10. The Philadelphia story: the 22q11.2 deletion: report on 250 patients. McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425 [TBL] [Abstract][Full Text] [Related]
12. FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities. Yakut T; Kilic SS; Cil E; Yapici E; Egeli U Pediatr Surg Int; 2006 Apr; 22(4):380-3. PubMed ID: 16463032 [TBL] [Abstract][Full Text] [Related]
13. Transient effect of anti-CD20 therapy in a child with 22q11.2 deletion syndrome and severe steroid refractory cytopenias: a case report. Soldatou A; Anastassiou T; Vougiouka O; Goussetis E; Kossiva L J Pediatr Hematol Oncol; 2013 May; 35(4):311-4. PubMed ID: 23612383 [TBL] [Abstract][Full Text] [Related]
14. Uveitis in DiGeorge syndrome: a case of autoimmune ocular inflammation in a patient with deletion 22q11.2. Gottlieb C; Li Z; Uzel G; Nussenblatt RB; Sen HN Ophthalmic Genet; 2010 Mar; 31(1):24-9. PubMed ID: 20141355 [TBL] [Abstract][Full Text] [Related]
15. The 22q11.2 deletion syndrome: more answers but more questions. Fernhoff PM J Pediatr; 2000 Aug; 137(2):145-7. PubMed ID: 10931401 [No Abstract] [Full Text] [Related]