415 related articles for article (PubMed ID: 18580689)
1. Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management.
Lin AE; Basson CT; Goldmuntz E; Magoulas PL; McDermott DA; McDonald-McGinn DM; McPherson E; Morris CA; Noonan J; Nowak C; Pierpont ME; Pyeritz RE; Rope AF; Zackai E; Pober BR
Genet Med; 2008 Jul; 10(7):469-94. PubMed ID: 18580689
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Pregnancy outcomes after assisted human reproduction.
Okun N; Sierra S; ;
J Obstet Gynaecol Can; 2014 Jan; 36(1):64-83. PubMed ID: 24444289
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [Prenatal diagnosis of conotruncal heart diseases. Results in 337 cases].
Boudjemline Y; Fermont L; Le Bidois J; Fraisse A; Kachaner J; Villain E; Sidi D; Bonnet D
Arch Mal Coeur Vaiss; 2000 May; 93(5):583-6. PubMed ID: 10858856
[TBL] [Abstract][Full Text] [Related]
7. Aberrant subclavian artery origin in tetralogy of Fallot with pulmonary stenosis is associated with chromosomal or genetic abnormality.
Oswal N; Christov G; Sridharan S; Khambadkone S; Bull C; Sullivan I
Cardiol Young; 2014 Jun; 24(3):478-84. PubMed ID: 23732114
[TBL] [Abstract][Full Text] [Related]
8. The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study.
Agergaard P; Olesen C; Østergaard JR; Christiansen M; Sørensen KM
Am J Med Genet A; 2012 Mar; 158A(3):498-508. PubMed ID: 22190294
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe.
Stoll C; Garne E; Clementi M;
Prenat Diagn; 2001 Apr; 21(4):243-52. PubMed ID: 11288111
[TBL] [Abstract][Full Text] [Related]
10. [Fetal atrioventricular septal defect associated with Patau and Edwards syndromes, as well as trisomy 22].
Cesko I; Hajdú J; Marton T; Tóth-Pál E; Papp C; Papp Z
Orv Hetil; 1998 May; 139(18):1087-9. PubMed ID: 9608772
[TBL] [Abstract][Full Text] [Related]
11. Spectrum of congenital heart defects and extracardiac malformations associated with chromosomal abnormalities: results of a seven year necropsy study.
Tennstedt C; Chaoui R; Körner H; Dietel M
Heart; 1999 Jul; 82(1):34-9. PubMed ID: 10377306
[TBL] [Abstract][Full Text] [Related]
12. Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations.
Shooner KA; Rope AF; Hopkin RJ; Andelfinger GU; Benson DW
J Pediatr; 2005 Mar; 146(3):382-7. PubMed ID: 15756225
[TBL] [Abstract][Full Text] [Related]
13. [Medical genetics and its goals].
Dallaire L
Union Med Can; 1972 Dec; 101(12):2663-8. PubMed ID: 4267672
[No Abstract] [Full Text] [Related]
14. Chromosomal abnormalities among children born with conotruncal cardiac defects.
Lammer EJ; Chak JS; Iovannisci DM; Schultz K; Osoegawa K; Yang W; Carmichael SL; Shaw GM
Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405
[TBL] [Abstract][Full Text] [Related]
15. Chromosomal and cardiovascular anomalies associated with congenital laryngeal web.
McElhinney DB; Jacobs I; McDonald-McGinn DM; Zackai EH; Goldmuntz E
Int J Pediatr Otorhinolaryngol; 2002 Oct; 66(1):23-27. PubMed ID: 12363418
[TBL] [Abstract][Full Text] [Related]
16. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
Vaz SO; Pires R; Pires LM; Carreira IM; Anjos R; Maciel P; Mota-Vieira L
BMC Pediatr; 2015 Aug; 15():95. PubMed ID: 26297018
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population.
Kong CW; Cheng YKY; To WWK; Leung TY
Hong Kong Med J; 2019 Feb; 25(1):6-12. PubMed ID: 30655461
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography.
Bellucco FT; Belangero SI; Farah LM; Machado MV; Cruz AP; Lopes LM; Lopes MA; Zugaib M; Cernach MC; Melaragno MI
Pediatr Cardiol; 2010 Nov; 31(8):1146-50. PubMed ID: 20848279
[TBL] [Abstract][Full Text] [Related]
20. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
Webber SA; Hatchwell E; Barber JC; Daubeney PE; Crolla JA; Salmon AP; Keeton BR; Temple IK; Dennis NR
J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]