526 related articles for article (PubMed ID: 8757559)
1. 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]
2. Anatomic patterns of conotruncal defects associated with deletion 22q11.
Marino B; Digilio MC; Toscano A; Anaclerio S; Giannotti A; Feltri C; de Ioris MA; Angioni A; Dallapiccola B
Genet Med; 2001; 3(1):45-8. PubMed ID: 11339377
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Counseling families with chromosome 22q11 deletions: the catch in CATCH-22.
Bristow JD; Bernstein HS
J Am Coll Cardiol; 1998 Aug; 32(2):499-501. PubMed ID: 9708482
[No Abstract] [Full Text] [Related]
11. 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]
12. Chromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries.
Aggarwal V; Imamura M; Acuna C; Cabrera AG
Cardiol Young; 2018 Mar; 28(3):467-470. PubMed ID: 29233233
[TBL] [Abstract][Full Text] [Related]
13. 22q11.2 deletion detected by
Ramírez-Velazco A; Rivera H; Vásquez-Velázquez AI; Aguayo-Orozco TA; Delgadillo-Pérez S; Domínguez MG
Colomb Med (Cali); 2018 Sep; 49(3):219-222. PubMed ID: 30410196
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Persistent fifth aortic arch associated with 22q11.2 deletion syndrome.
Lee ML; Chen HN; Chen M; Tsao LY; Wang BT; Lee MH; Chiu IS
J Formos Med Assoc; 2006 Apr; 105(4):284-9. PubMed ID: 16618608
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
Ravnan JB; Chen E; Golabi M; Lebo RV
Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
[TBL] [Abstract][Full Text] [Related]
19. Interruption of the aortic arch at the isthmus with DiGeorge syndrome and 22q11.2 deletion.
Takahashi K; Kuwahara T; Nagatsu M
Cardiol Young; 1999 Sep; 9(5):516-8. PubMed ID: 10535835
[TBL] [Abstract][Full Text] [Related]
20. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
Momma K; Matsuoka R; Takao A
Pediatr Cardiol; 1999; 20(2):97-102. PubMed ID: 9986884
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]