545 related articles for article (PubMed ID: 19224675)
1. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
Hu Y; Zhu X; Yang Y; Mo X; Sheng M; Yao J; Wang D
Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
[TBL] [Abstract][Full Text] [Related]
2. [Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation dependent probe amplification].
Yang YH; Hu YL; Zhu XY; Mo XM; Wang DJ; Yao JC; Sheng M; Zhu HY; Li J; Ru T; Wang ZQ
Zhongguo Dang Dai Er Ke Za Zhi; 2009 Nov; 11(11):892-6. PubMed ID: 20113655
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. [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]
6. [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]
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. Concurrent microdeletion and duplication of 22q11.2.
Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations.
Yang C; Shen L; Xu Z; Wu X; Mo X; Zhang J; Wang D; Wang Y; Peng Y; Cao L; Jiang Y; Gu H; Chen S; Bian X; Liu J; Qiao D; Yi L
Electrophoresis; 2009 Feb; 30(3):465-71. PubMed ID: 19145597
[TBL] [Abstract][Full Text] [Related]
11. [Clinical detection of 22q11 microdeletion in the patients with congenital heart disease by multiplex ligation dependent probe amplification].
Chen Y; Kan HJ; Mao J; Ding J; Meng QX; Li HB; Cheng HB; Liu MJ; Sun Y; Yan WH; Li H
Zhonghua Er Ke Za Zhi; 2011 Apr; 49(4):316-9. PubMed ID: 21624212
[TBL] [Abstract][Full Text] [Related]
12. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
[TBL] [Abstract][Full Text] [Related]
13. Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
Pires R; Pires LM; Vaz SO; Maciel P; Anjos R; Moniz R; Branco CC; Cabral R; Carreira IM; Mota-Vieira L
BMC Genet; 2014 Nov; 15():115. PubMed ID: 25376777
[TBL] [Abstract][Full Text] [Related]
14. 22q11.2 deletion syndrome in Singapore (2000-2003): a case for active ascertainment.
Tan KB; Chew SK; Yeo GS
Singapore Med J; 2008 Apr; 49(4):286-9. PubMed ID: 18418519
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].
Luo CY; Ma DY; Zhang JJ; Hu P; Cao L; Ji XQ; Zhou J; Liu A; Wu Y; Cheng J; Lin Y; Xu ZF
Zhonghua Fu Chan Ke Za Zhi; 2013 Nov; 48(11):824-7. PubMed ID: 24444558
[TBL] [Abstract][Full Text] [Related]
17. Congenital cardiac defects with 22q11 deletion.
Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D
Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
[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. 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]
20. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
