These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
203 related articles for article (PubMed ID: 16761295)
21. 22q11.2 microdeletion syndrome is a common cause of renal tract malformations. Burtey S Nat Clin Pract Nephrol; 2008 Aug; 4(8):E1. PubMed ID: 18654600 [No Abstract] [Full Text] [Related]
22. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases. Vaz SO; Pires R; Pires LM; Carreira IM; Anjos R; Maciel P; Mota-Vieira L BMC Pediatr; 2015 Aug; 15():95. PubMed ID: 26297018 [TBL] [Abstract][Full Text] [Related]
24. A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients. Erickson RP; Díaz de Ståhl T; Bruder CE; Dumanski JP Am J Med Genet A; 2007 Dec; 143A(24):3302-8. PubMed ID: 18000907 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11. Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461 [TBL] [Abstract][Full Text] [Related]
27. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion. Bartsch O; Nemecková M; Kocárek E; Wagner A; Puchmajerová A; Poppe M; Ounap K; Goetz P Am J Med Genet A; 2003 Feb; 117A(1):1-5. PubMed ID: 12548732 [TBL] [Abstract][Full Text] [Related]
28. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma. Tarlan B; Kiratli H; Kılıç E; Utine E; Boduroğlu K Ophthalmic Genet; 2014 Dec; 35(4):248-51. PubMed ID: 23834556 [TBL] [Abstract][Full Text] [Related]
29. [Genotype and phenotype study of two patients with 22q11.2 deletion syndrome]. Zhu H; Wang A; Zhang H; Ji C; Zhan X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):623-7. PubMed ID: 25297596 [TBL] [Abstract][Full Text] [Related]
30. Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects. Funke B; Epstein JA; Kochilas LK; Lu MM; Pandita RK; Liao J; Bauerndistel R; Schüler T; Schorle H; Brown MC; Adams J; Morrow BE Hum Mol Genet; 2001 Oct; 10(22):2549-56. PubMed ID: 11709542 [TBL] [Abstract][Full Text] [Related]
31. Phenotypic variability of atypical 22q11.2 deletions not including TBX1. Verhagen JM; Diderich KE; Oudesluijs G; Mancini GM; Eggink AJ; Verkleij-Hagoort AC; Groenenberg IA; Willems PJ; du Plessis FA; de Man SA; Srebniak MI; van Opstal D; Hulsman LO; van Zutven LJ; Wessels MW Am J Med Genet A; 2012 Oct; 158A(10):2412-20. PubMed ID: 22893440 [TBL] [Abstract][Full Text] [Related]
32. Chromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries. Aggarwal V; Imamura M; Acuna C; Cabrera AG Cardiol Young; 2018 Mar; 28(3):467-470. PubMed ID: 29233233 [TBL] [Abstract][Full Text] [Related]
33. Atypical 22q11.2 Microduplication with "Typical" Signs and Overgrowth. Fischer M; Klopocki E Cytogenet Genome Res; 2020; 160(11-12):659-663. PubMed ID: 33472199 [TBL] [Abstract][Full Text] [Related]
34. Deletion 22q11 syndrome: acknowledging a lost eponym as we say farewell to an acronym. Turnpenny PD; Pigott RW J Med Genet; 2001 Apr; 38(4):271-3. PubMed ID: 11370635 [No Abstract] [Full Text] [Related]
35. Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region. Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J Eur J Pediatr Surg; 1993 Dec; 3 Suppl 1():27-8. PubMed ID: 8130147 [No Abstract] [Full Text] [Related]
36. Clinical correlation of chromosome 22q11.2 fluorescent in situ hybridization analysis and velocardiofacial syndrome. Oh AK; Workman LA; Wong GB Cleft Palate Craniofac J; 2007 Jan; 44(1):62-6. PubMed ID: 17214538 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers. Shetty M; Srikanth A; Kadandale J; Hegde S Cytogenet Genome Res; 2016; 148(4):249-55. PubMed ID: 27300488 [TBL] [Abstract][Full Text] [Related]