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.
126 related articles for article (PubMed ID: 11339381)
1. 22q11.2 microdeletions in adults with familial tetralogy of Fallot. Hokanson JS; Pierpont E; Hirsch B; Moller JH Genet Med; 2001; 3(1):61-4. PubMed ID: 11339381 [TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion. Oh DC; Min JY; Lee MH; Kim YM; Park SY; Won HS; Kim IK; Lee YH; Yoo SJ; Ryu HM J Korean Med Sci; 2002 Feb; 17(1):125-8. PubMed ID: 11850602 [TBL] [Abstract][Full Text] [Related]
4. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion. Momma K; Kondo C; Matsuoka R J Am Coll Cardiol; 1996 Jan; 27(1):198-202. PubMed ID: 8522695 [TBL] [Abstract][Full Text] [Related]
5. Chromosomal abnormalities among children born with conotruncal cardiac defects. Lammer EJ; Chak JS; Iovannisci DM; Schultz K; Osoegawa K; Yang W; Carmichael SL; Shaw GM Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405 [TBL] [Abstract][Full Text] [Related]
6. Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults. Momma K; Takao A; Matsuoka R; Imai Y; Muto A; Osawa M; Takayama M Genet Med; 2001; 3(1):56-60. PubMed ID: 11339379 [TBL] [Abstract][Full Text] [Related]
7. Frequent association of 22q11.2 deletion with tetralogy of Fallot. Maeda J; Yamagishi H; Matsuoka R; Ishihara J; Tokumura M; Fukushima H; Ueda H; Takahashi E; Yoshiba S; Kojima Y Am J Med Genet; 2000 Jun; 92(4):269-72. PubMed ID: 10842294 [TBL] [Abstract][Full Text] [Related]
8. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland. Wozniak A; Wolnik-Brzozowska D; Wisniewska M; Glazar R; Materna-Kiryluk A; Moszura T; Badura-Stronka M; Skolozdrzy J; Krawczynski MR; Zeyland J; Bobkowski W; Slomski R; Latos-Bielenska A; Siwinska A BMC Pediatr; 2010 Dec; 10():88. PubMed ID: 21134246 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Study on the relationship between 22q11 microdeletion and congenital heart disease]. Du YR; Yang HJ; Tan Z; Huang Y; Li SL; Tian JW; Zhang GY; Li P; Fu SB Yi Chuan; 2005 Nov; 27(6):873-6. PubMed ID: 16378931 [TBL] [Abstract][Full Text] [Related]
11. Prevalence and parental origin in Tetralogy of Fallot associated with chromosome 22q11 microdeletion. Lu JH; Chung MY; Hwang B; Chien HP Pediatrics; 1999 Jul; 104(1 Pt 1):87-90. PubMed ID: 10390265 [TBL] [Abstract][Full Text] [Related]
12. [Microdeletion of 22q11 and conotruncal cardiopathies: contribution of prenatal diagnosis]. Verspyck E; Joly G; Rossi A; David N; Blaysat G; Henocq A; Moirot H; Labadie G; Marpeau L J Gynecol Obstet Biol Reprod (Paris); 1999 Oct; 28(6):534-7. PubMed ID: 10598346 [TBL] [Abstract][Full Text] [Related]
13. Tetralogy of Fallot associated with chromosome 22q11 deletion. Momma K; Kondo C; Ando M; Matsuoka R; Takao A Am J Cardiol; 1995 Sep; 76(8):618-21. PubMed ID: 7677092 [No Abstract] [Full Text] [Related]
14. [Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease]. Salazar M; Villalba G; Mateus H; Villegas V; Fonseca D; Núñez F; Caicedo V; Pachón S; Bernal JE Invest Clin; 2011 Dec; 52(4):334-43. PubMed ID: 22523843 [TBL] [Abstract][Full Text] [Related]
15. [Chromosome 22q11.2 microdeletion and phenotype analysis of patients with non-syndromic tetralogy of Fallot]. Zhang ZW; Deng JY; Ying LY; Gao Z; Jin J; Qi JC; Tan Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):708-11. PubMed ID: 22161111 [TBL] [Abstract][Full Text] [Related]
16. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia. van Engelen K; Topf A; Keavney BD; Goodship JA; van der Velde ET; Baars MJ; Snijder S; Moorman AF; Postma AV; Mulder BJ Heart; 2010 Apr; 96(8):621-4. PubMed ID: 20357389 [TBL] [Abstract][Full Text] [Related]
17. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study. Webber SA; Hatchwell E; Barber JC; Daubeney PE; Crolla JA; Salmon AP; Keeton BR; Temple IK; Dennis NR J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559 [TBL] [Abstract][Full Text] [Related]
18. Familial absent pulmonary valve syndrome without deletions of chromosome 22q11. McElhinney DB; Hanley FL; Stanger P Cardiol Young; 2000 Nov; 10(6):618-20. PubMed ID: 11117395 [TBL] [Abstract][Full Text] [Related]
19. Influence of chromosome 22q11.2 microdeletion on surgical outcome after treatment of tetralogy of fallot with pulmonary atresia. Carotti A; Marino B; Di Donato RM J Thorac Cardiovasc Surg; 2003 Nov; 126(5):1666-7. PubMed ID: 14666061 [No Abstract] [Full Text] [Related]
20. Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot. Carli D; Moroni A; Eleonora DG; Zonta A; Montin D; Licciardi F; Aidala E; Bordese R; Carlo PN; Brusco A; Giovanni Battista F; Mussa A J Genet; 2021; 100():. PubMed ID: 33707356 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]