198 related articles for article (PubMed ID: 11295715)
1. 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]
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. 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. 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. [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]
6. Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects.
Chaoui R; Kalache KD; Heling KS; Tennstedt C; Bommer C; Körner H
Ultrasound Obstet Gynecol; 2002 Dec; 20(6):546-52. PubMed ID: 12493042
[TBL] [Abstract][Full Text] [Related]
7. [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]
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. 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]
10. 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]
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. 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]
13. 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]
14. Cardiovascular malformations among preterm infants.
Tanner K; Sabrine N; Wren C
Pediatrics; 2005 Dec; 116(6):e833-8. PubMed ID: 16322141
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. [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]
19. 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]
20. [22q11 deletion in conotruncal anomalies].
Kádár K
Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]