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27. 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]
28. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients. Borgmann S; Luhmer I; Arslan-Kirchner M; Kallfelz HC; Schmidtke J Eur J Pediatr; 1999 Dec; 158(12):958-63. PubMed ID: 10592069 [TBL] [Abstract][Full Text] [Related]
29. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience. Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191 [TBL] [Abstract][Full Text] [Related]
30. Congenital cardiac defects with 22q11 deletion. Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. [Relationship between 22q11 microdeletion syndrome and congenital heart disease]. Qin YF; Xie CH; Yang JB; Wu DW; Shao J; Zhao ZY Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Jul; 39(7):631-5. PubMed ID: 22088244 [TBL] [Abstract][Full Text] [Related]
33. Molecular characterization of chromosome 22 deletions by short tandem repeat polymorphism (STRP) in patients with conotruncal heart defects. Vittorini S; Sacchelli M; Iascone MR; Collavoli A; Storti S; Giusti A; Andreani G; Botto N; Biagini A; Clerico A Clin Chem Lab Med; 2001 Dec; 39(12):1249-58. PubMed ID: 11798086 [TBL] [Abstract][Full Text] [Related]
34. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome. Momma K; Kondo C; Matsuoka R; Takao A Am J Cardiol; 1996 Sep; 78(5):591-4. PubMed ID: 8806353 [TBL] [Abstract][Full Text] [Related]
35. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions. Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167 [TBL] [Abstract][Full Text] [Related]
36. Chromosome 22q11 microdeletion in conotruncal heart defects: clinical presentation, parental origin and de novo mutations. Chung MY; Lu JH; Chien HP; Hwang B Int J Mol Med; 2001 May; 7(5):501-5. PubMed ID: 11295111 [TBL] [Abstract][Full Text] [Related]
37. Chromosome 22q11 microdeletion and congenital heart disease--a survey in a paediatric population. Yong DE; Booth P; Baruni J; Massie D; Stephen G; Couzin D; Dean JC Eur J Pediatr; 1999 Jul; 158(7):566-70. PubMed ID: 10412816 [TBL] [Abstract][Full Text] [Related]
38. Screening of patients at risk for 22q11 deletion. Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202 [TBL] [Abstract][Full Text] [Related]
39. Mosaic 22q11.2 deletion and tetralogy of Fallot with absent pulmonary valve: an unreported association. Prabhu S; Jenny B; James H; Provenzano S World J Pediatr Congenit Heart Surg; 2015 Apr; 6(2):342-5. PubMed ID: 25870364 [TBL] [Abstract][Full Text] [Related]
40. [Frequency of 22q11 deletions in children with isolated conotruncal defects]. Shen L; Xu YJ; Zhao PJ; Sun K Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jan; 11(1):25-8. PubMed ID: 19149917 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]