260 related articles for article (PubMed ID: 30410196)
1. 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]
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. 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]
4. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
Wozniak A; Wolnik-Brzozowska D; Wisniewska M; Glazar R; Materna-Kiryluk A; Moszura T; Badura-Stronka M; Skolozdrzy J; Krawczynski MR; Zeyland J; Bobkowski W; Slomski R; Latos-Bielenska A; Siwinska A
BMC Pediatr; 2010 Dec; 10():88. PubMed ID: 21134246
[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. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
[TBL] [Abstract][Full Text] [Related]
7. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
Huber J; Peres VC; de Castro AL; dos Santos TJ; da Fontoura Beltrão L; de Baumont AC; Cossio SL; Dalberto TP; Riegel M; Cañedo AD; Schaan BD; Pellanda LC
Pediatr Cardiol; 2014 Dec; 35(8):1356-62. PubMed ID: 24880467
[TBL] [Abstract][Full Text] [Related]
10. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.
Bartsch O; Nemecková M; Kocárek E; Wagner A; Puchmajerová A; Poppe M; Ounap K; Goetz P
Am J Med Genet A; 2003 Feb; 117A(1):1-5. PubMed ID: 12548732
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. Frequent association of 22q11.2 deletion with tetralogy of Fallot.
Maeda J; Yamagishi H; Matsuoka R; Ishihara J; Tokumura M; Fukushima H; Ueda H; Takahashi E; Yoshiba S; Kojima Y
Am J Med Genet; 2000 Jun; 92(4):269-72. PubMed ID: 10842294
[TBL] [Abstract][Full Text] [Related]
14. Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.
Fung WL; Chow EW; Webb GD; Gatzoulis MA; Bassett AS
Int J Cardiol; 2008 Dec; 131(1):51-8. PubMed ID: 18191243
[TBL] [Abstract][Full Text] [Related]
15. 22q11.2 deletion syndrome and congenital heart disease.
Goldmuntz E
Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):64-72. PubMed ID: 32049433
[TBL] [Abstract][Full Text] [Related]
16. 22q11.2 Deletion Syndrome in Taiwan: Clinical Presentation and Immune System Status of Patients.
Lee CL; Lin SM; Chen MR; Chuang CK; Chiu HC; Tu YR; Lo YT; Chang YH; Lin HY; Lin SP
Int J Med Sci; 2023; 20(11):1377-1385. PubMed ID: 37790845
[No Abstract] [Full Text] [Related]
17. Genetic basis of DiGeorge and velocardiofacial syndromes.
Driscoll DA
Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818
[TBL] [Abstract][Full Text] [Related]
18. FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.
Yakut T; Kilic SS; Cil E; Yapici E; Egeli U
Pediatr Surg Int; 2006 Apr; 22(4):380-3. PubMed ID: 16463032
[TBL] [Abstract][Full Text] [Related]
19. Towards earlier diagnosis of 22q11 deletions.
Tobias ES; Morrison N; Whiteford ML; Tolmie JL
Arch Dis Child; 1999 Dec; 81(6):513-4. PubMed ID: 10569971
[TBL] [Abstract][Full Text] [Related]
20. Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot.
Carli D; Moroni A; Eleonora DG; Zonta A; Montin D; Licciardi F; Aidala E; Bordese R; Carlo PN; Brusco A; Giovanni Battista F; Mussa A
J Genet; 2021; 100():. PubMed ID: 33707356
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
