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.
305 related articles for article (PubMed ID: 8230162)
1. DiGeorge syndrome: part of CATCH 22. Wilson DI; Burn J; Scambler P; Goodship J J Med Genet; 1993 Oct; 30(10):852-6. PubMed ID: 8230162 [TBL] [Abstract][Full Text] [Related]
2. 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]
4. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations. Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620 [TBL] [Abstract][Full Text] [Related]
5. "CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency? Lipson A; Emanuel B; Colley P; Fagan K; Driscoll DA J Med Genet; 1994 Sep; 31(9):741. PubMed ID: 7815448 [No Abstract] [Full Text] [Related]
7. 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; 96(6):419-23. PubMed ID: 9216164 [TBL] [Abstract][Full Text] [Related]
9. 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; 53(3):285-9. PubMed ID: 7856665 [TBL] [Abstract][Full Text] [Related]
11. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes. Crifasi PA; Michels VV; Driscoll DJ; Jalal SM; Dewald GW Mayo Clin Proc; 1995 Dec; 70(12):1148-53. PubMed ID: 7490915 [TBL] [Abstract][Full Text] [Related]
12. [Teleradiographic analysis of velopharyngeal insufficiency in CATCH 22 association]. Houze de L'Aulnoit S; Martinot V; Breviere GM; Kulik JF; Pellerin P Ann Chir Plast Esthet; 1999 Oct; 44(5):525-30. PubMed ID: 10609375 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Closing time for CATCH22. Burn J J Med Genet; 1999 Oct; 36(10):737-8. PubMed ID: 10528851 [No Abstract] [Full Text] [Related]
15. 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; 99(5):E9. PubMed ID: 9113966 [TBL] [Abstract][Full Text] [Related]
16. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features. Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900 [TBL] [Abstract][Full Text] [Related]
17. Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects. Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C Dev Med Child Neurol; 2002 Jan; 44(1):44-50. PubMed ID: 11811651 [TBL] [Abstract][Full Text] [Related]
18. DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case. Wang JL; Chen SJ; Chung MY; Niu DM; Lin CY; Hwang BT; Lu JH Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(5):385-9. PubMed ID: 9401184 [TBL] [Abstract][Full Text] [Related]
19. Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome. Seaver LH; Pierpont JW; Erickson RP; Donnerstein RL; Cassidy SB J Med Genet; 1994 Nov; 31(11):830-4. PubMed ID: 7853364 [TBL] [Abstract][Full Text] [Related]