257 related articles for article (PubMed ID: 22088244)
1. [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]
2. 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]
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. [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]
5. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
Qin YF; Yang JB; Xie CH; Shao J; Zhao ZY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Genetic background of congenital conotruncal heart defects--a study of 45 families.
Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
[TBL] [Abstract][Full Text] [Related]
8. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. 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]
14. Microdeletion 22q11 and oesophageal atresia.
Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. [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]
17. 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]
18. 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]
19. 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]
20. [22q11.2 deletion syndrome and complex congenital heart defects].
Rosa RF; Trevisan P; Koshiyama DB; Pilla CB; Zen PR; Varella-Garcia M; Paskulin GA
Rev Assoc Med Bras (1992); 2011; 57(1):62-5. PubMed ID: 21390462
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]