356 related articles for article (PubMed ID: 16575883)
1. 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]
2. [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]
3. 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]
4. 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]
5. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].
Xu ZF; Yi L; Mo XM; Hu Y; Wang DJ; Zhu RF; Jiang YZ; Wu X; Wu Z; Shen L; Zhang Y; Zhong XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):250-5. PubMed ID: 16767657
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. [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]
9. 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]
10. 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]
11. Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases.
Gioli-Pereira L; Pereira AC; Bergara D; Mesquita S; Lopes AA; Krieger JE
Int J Cardiol; 2008 Jun; 126(3):374-8. PubMed ID: 17604138
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. [22q11 deletion in conotruncal anomalies].
Kádár K
Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Co-occurrence of chromosome 22q11.2 microdeletion and trisomy 21 mosaicism.
Derbent M; Saygili A; Yilmaz Z; Kervancioğlu M; Balci S; Tokel K
Am J Med Genet; 2002 Sep; 112(1):99-102. PubMed ID: 12239730
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]