447 related articles for article (PubMed ID: 15803887)
1. [22q11 deletion in conotruncal anomalies].
Kádár K
Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
Beauchesne LM; Warnes CA; Connolly HM; Ammash NM; Grogan M; Jalal SM; Michels VV
J Am Coll Cardiol; 2005 Feb; 45(4):595-8. PubMed ID: 15708709
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. [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]
6. [Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].
Buendía Hernández A; Calderón-Colmenero J; Aizpuru E; Attie CL; Zabal C; Patiño E; Miranda I; Juanico A; Attie F
Arch Inst Cardiol Mex; 2000; 70(2):148-53. PubMed ID: 10932799
[TBL] [Abstract][Full Text] [Related]
7. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
Carotti A; Digilio MC; Piacentini G; Saffirio C; Di Donato RM; Marino B
Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
[TBL] [Abstract][Full Text] [Related]
8. Chromosome 22q11 deletions in patients with conotruncal heart defects.
Khositseth A; Tocharoentanaphol C; Khowsathit P; Ruangdaraganon N
Pediatr Cardiol; 2005; 26(5):570-3. PubMed ID: 16132309
[TBL] [Abstract][Full Text] [Related]
9. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
Soares G; Alvares S; Rocha C; Teixeira MF; Mota MC; Reis MI; Feijó MJ; Lima MR; Pinto MR
Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
[TBL] [Abstract][Full Text] [Related]
10. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
Momma K; Matsuoka R; Takao A
Pediatr Cardiol; 1999; 20(2):97-102. PubMed ID: 9986884
[TBL] [Abstract][Full Text] [Related]
11. Frequency of 22q11 deletions in patients with conotruncal defects.
Goldmuntz E; Clark BJ; Mitchell LE; Jawad AF; Cuneo BF; Reed L; McDonald-McGinn D; Chien P; Feuer J; Zackai EH; Emanuel BS; Driscoll DA
J Am Coll Cardiol; 1998 Aug; 32(2):492-8. PubMed ID: 9708481
[TBL] [Abstract][Full Text] [Related]
12. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
Frohn-Mulder IM; Wesby Swaay E; Bouwhuis C; Van Hemel JO; Gerritsma E; Niermeyer MF; Hess J
Genet Couns; 1999; 10(1):35-41. PubMed ID: 10191427
[TBL] [Abstract][Full Text] [Related]
13. Anatomic patterns of conotruncal defects associated with deletion 22q11.
Marino B; Digilio MC; Toscano A; Anaclerio S; Giannotti A; Feltri C; de Ioris MA; Angioni A; Dallapiccola B
Genet Med; 2001; 3(1):45-8. PubMed ID: 11339377
[TBL] [Abstract][Full Text] [Related]
14. 22q11.2 deletion mosaicism in patients with conotruncal heart defects.
Jianrong L; Yinglong L; Xiaodong L; Cuntao Y; Bin C; Bo W
Birth Defects Res A Clin Mol Teratol; 2006 Apr; 76(4):262-5. PubMed ID: 16575883
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
Ziolkowska L; Kawalec W; Turska-Kmiec A; Krajewska-Walasek M; Brzezinska-Rajszys G; Daszkowska J; Maruszewski B; Burczynski P
Eur J Pediatr; 2008 Oct; 167(10):1135-40. PubMed ID: 18172682
[TBL] [Abstract][Full Text] [Related]
16. Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?
Rauch R; Rauch A; Koch A; Zink S; Kaulitz R; Girisch M; Singer H; Hofbeck M
Eur J Pediatr; 2004 Nov; 163(11):642-5. PubMed ID: 15300432
[TBL] [Abstract][Full Text] [Related]
17. Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndrome.
Devriendt K; Van Schoubroeck D; Eyskens B; Vantrappen G; Swillen A; Gewillig M; Dumoulin M; Moerman P; Vandenberghe K; Fryns JP
Prenat Diagn; 1998 Jan; 18(1):68-72. PubMed ID: 9483643
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.
Boudjemline Y; Fermont L; Le Bidois J; Lyonnet S; Sidi D; Bonnet D
J Pediatr; 2001 Apr; 138(4):520-4. PubMed ID: 11295715
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Search for 22q11 deletion and linkage study in familial cases of non-syndromic conotruncal defects].
Debrus S
Arch Mal Coeur Vaiss; 1994 May; 87(5):657-61. PubMed ID: 7857190
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]