284 related articles for article (PubMed ID: 9099830)
1. Microdeletion 22q11 in complex cardiovascular malformations.
Mehraein Y; Wippermann CF; Michel-Behnke I; Nhan Ngo TK; Hillig U; Giersberg M; Aulepp U; Barth H; Fritz B; Rehder H
Hum Genet; 1997 Apr; 99(4):433-42. PubMed ID: 9099830
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?
Rauch R; Rauch A; Koch A; Zink S; Kaulitz R; Girisch M; Singer H; Hofbeck M
Eur J Pediatr; 2004 Nov; 163(11):642-5. PubMed ID: 15300432
[TBL] [Abstract][Full Text] [Related]
7. [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]
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. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.
Momma K; Kondo C; Matsuoka R; Takao A
Am J Cardiol; 1996 Sep; 78(5):591-4. PubMed ID: 8806353
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.
Crifasi PA; Michels VV; Driscoll DJ; Jalal SM; Dewald GW
Mayo Clin Proc; 1995 Dec; 70(12):1148-53. PubMed ID: 7490915
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. [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]
20. Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion.
Akçakuş M; Güneş T; Kurtoğlu S; Cetin N; Ozkul Y; Narin N; Atabek ME; Uğraş R
Turk J Pediatr; 2004; 46(2):191-3. PubMed ID: 15214756
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
