207 related articles for article (PubMed ID: 1747284)
1. DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.
Wilson DI; Cross IE; Goodship JA; Coulthard S; Carey AH; Scambler PJ; Bain HH; Hunter AS; Carter PE; Burn J
Br Heart J; 1991 Oct; 66(4):308-12. PubMed ID: 1747284
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
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. Isolated innominate artery in 22q11 microdeletion.
Duke C; Chan KC
Pediatr Cardiol; 2001; 22(1):80-2. PubMed ID: 11123139
[TBL] [Abstract][Full Text] [Related]
7. Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients.
Momma K; Ando M; Matsuoka R; Joo K
Cardiol Young; 1999 Sep; 9(5):463-7. PubMed ID: 10535824
[TBL] [Abstract][Full Text] [Related]
8. Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies.
Toscano A; Anaclerio S; Digilio MC; Giannotti A; Fariello G; Dallapiccola B; Marino B
Eur J Pediatr; 2002 Feb; 161(2):116-7. PubMed ID: 11954747
[No Abstract] [Full Text] [Related]
9. The genetic implication for preceding generations of the prenatal diagnosis of interrupted aortic arch in association with unsuspected DiGeorge anomaly.
Puder KS; Humes RA; Gold RL; Bawle EV; Goyert GL
Am J Obstet Gynecol; 1995 Jul; 173(1):239-41. PubMed ID: 7631695
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns.
Anaclerio S; Marino B; Carotti A; Digilio MC; Toscano A; Gitto P; Giannotti A; Di Donato R; Dallapiccola B
Ital Heart J; 2001 May; 2(5):384-7. PubMed ID: 11392644
[TBL] [Abstract][Full Text] [Related]
12. The Subtlety of 22q11.2 Deletion Syndrome in a Preterm Neonate.
Cline L; Aranda P; Jnah A
Neonatal Netw; 2023 Jun; 42(3):137-144. PubMed ID: 37258294
[TBL] [Abstract][Full Text] [Related]
13. DiGeorge syndrome: clinical variability in a family with submicroscopic deletion at 22q11.2.
Tsui KM; Ng YY; Lam TS
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(1):52-6. PubMed ID: 9066191
[TBL] [Abstract][Full Text] [Related]
14. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
15. Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11.
Carey AH; Claussen U; Lüdecke HJ; Horsthemke B; Ellis D; Oakey H; Wilson D; Burn J; Williamson R; Scambler PJ
Mamm Genome; 1992; 3(2):101-5. PubMed ID: 1617213
[TBL] [Abstract][Full Text] [Related]
16. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
Tarlan B; Kiratli H; Kılıç E; Utine E; Boduroğlu K
Ophthalmic Genet; 2014 Dec; 35(4):248-51. PubMed ID: 23834556
[TBL] [Abstract][Full Text] [Related]
17. Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case.
Hou JW; Wang JK; Chou CC; Wang TR
J Formos Med Assoc; 1995 Apr; 94(4):200-2. PubMed ID: 7606185
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies.
McElhinney DB; Driscoll DA; Levin ER; Jawad AF; Emanuel BS; Goldmuntz E
Pediatrics; 2003 Dec; 112(6 Pt 1):e472. PubMed ID: 14654648
[TBL] [Abstract][Full Text] [Related]
20. DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.
Wang JL; Chen SJ; Chung MY; Niu DM; Lin CY; Hwang BT; Lu JH
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(5):385-9. PubMed ID: 9401184
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
