383 related articles for article (PubMed ID: 20494672)
1. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome.
Momma K
Am J Cardiol; 2010 Jun; 105(11):1617-24. PubMed ID: 20494672
[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. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
Park IS; Ko JK; Kim YH; Yoo HW; Seo EJ; Choi JY; Gil HY; Kim SJ
Int J Cardiol; 2007 Jan; 114(2):230-5. PubMed ID: 16824627
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.
McElhinney DB; Clark BJ; Weinberg PM; Kenton ML; McDonald-McGinn D; Driscoll DA; Zackai EH; Goldmuntz E
J Am Coll Cardiol; 2001 Jun; 37(8):2114-9. PubMed ID: 11419896
[TBL] [Abstract][Full Text] [Related]
14. Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns.
Anaclerio S; Marino B; Carotti A; Digilio MC; Toscano A; Gitto P; Giannotti A; Di Donato R; Dallapiccola B
Ital Heart J; 2001 May; 2(5):384-7. PubMed ID: 11392644
[TBL] [Abstract][Full Text] [Related]
15. [22q11 deletion in conotruncal anomalies].
Kádár K
Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
[TBL] [Abstract][Full Text] [Related]
16. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
Iserin L; de Lonlay P; Viot G; Sidi D; Kachaner J; Munnich A; Lyonnet S; Vekemans M; Bonnet D
Eur J Pediatr; 1998 Nov; 157(11):881-4. PubMed ID: 9835429
[TBL] [Abstract][Full Text] [Related]
18. Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children.
Anilkumar A; Kappanayil M; Thampi MV; Nampoothiri S; Sundaram KR; Vasudevan DM
Acta Paediatr; 2011 Sep; 100(9):e97-100. PubMed ID: 21418101
[TBL] [Abstract][Full Text] [Related]
19. 22q11.2 deletion syndrome and congenital heart disease.
Goldmuntz E
Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):64-72. PubMed ID: 32049433
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
