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8. Genetic compensation in a human genomic disorder. Carelle-Calmels N; Saugier-Veber P; Girard-Lemaire F; Rudolf G; Doray B; Guérin E; Kuhn P; Arrivé M; Gilch C; Schmitt E; Fehrenbach S; Schnebelen A; Frébourg T; Flori E N Engl J Med; 2009 Mar; 360(12):1211-6. PubMed ID: 19297573 [TBL] [Abstract][Full Text] [Related]
9. DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome. Sullivan KE Adv Exp Med Biol; 2007; 601():37-49. PubMed ID: 17712990 [TBL] [Abstract][Full Text] [Related]
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11. Counseling families with chromosome 22q11 deletions: the catch in CATCH-22. Bristow JD; Bernstein HS J Am Coll Cardiol; 1998 Aug; 32(2):499-501. PubMed ID: 9708482 [No Abstract] [Full Text] [Related]
12. Deletion of 22q11 in two brothers with different phenotype. Kasprzak L; Der Kaloustian VM; Elliott AM; Shevell M; Lejtenyi C; Eydoux P Am J Med Genet; 1998 Jan; 75(3):288-91. PubMed ID: 9475599 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Views of adults with 22q11 deletion syndrome on reproductive choices. McNeill A; Lewis R; Freeth M Am J Med Genet A; 2020 May; 182(5):1284-1287. PubMed ID: 32154643 [No Abstract] [Full Text] [Related]
15. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279 [TBL] [Abstract][Full Text] [Related]
16. Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome). Kuo CY; Signer R; Saitta SC Curr Allergy Asthma Rep; 2018 Oct; 18(12):75. PubMed ID: 30377837 [TBL] [Abstract][Full Text] [Related]
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18. 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]
19. Preimplantation genetic diagnosis of DiGeorge syndrome. Iwarsson E; Ahrlund-Richter L; Inzunza J; Fridström M; Rosenlund B; Hillensjö T; Sjöblom P; Nordenskjöld M; Blennow E Mol Hum Reprod; 1998 Sep; 4(9):871-5. PubMed ID: 9783847 [TBL] [Abstract][Full Text] [Related]
20. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Bassett AS; Marshall CR; Lionel AC; Chow EW; Scherer SW Hum Mol Genet; 2008 Dec; 17(24):4045-53. PubMed ID: 18806272 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]