284 related articles for article (PubMed ID: 9777346)
1. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
Von Beust G; Bartmus D; Bartels I
Genet Couns; 1998; 9(3):223-7. PubMed ID: 9777346
[No Abstract] [Full Text] [Related]
2. 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]
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: a microdeletion of chromosome 22 behind the polymorphous syndrome].
Somer M; Ignatius J; Vehmanen P; Keinänen M; Haapanen ML
Duodecim; 1997; 113(12):1115-22. PubMed ID: 11466836
[No Abstract] [Full Text] [Related]
5. Genetic background of congenital conotruncal heart defects--a study of 45 families.
Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
[TBL] [Abstract][Full Text] [Related]
6. [CATCH 22].
Matsuo N; Yamagishi H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):150-3. PubMed ID: 11057175
[No Abstract] [Full Text] [Related]
7. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP
Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
[TBL] [Abstract][Full Text] [Related]
8. CATCHing a break on 22.
Glover TW
Nat Genet; 1995 Jul; 10(3):257-8. PubMed ID: 7670460
[No Abstract] [Full Text] [Related]
9. Congenital cardiac defects with 22q11 deletion.
Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D
Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
[TBL] [Abstract][Full Text] [Related]
10. CATCH 22 Syndrome.
Yonehara Y; Nakatsuka T; Ichioka S; Sasaki N; Kobayashi T
J Craniofac Surg; 2002 Sep; 13(5):623-6. PubMed ID: 12218787
[TBL] [Abstract][Full Text] [Related]
11. Screening of patients at risk for 22q11 deletion.
Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. CATCH 22: a possible cause of congenital unilateral facial nerve palsy.
Ehara H; Hara T; Takeshita K
Eur J Pediatr; 1997 Sep; 156(9):739. PubMed ID: 9296543
[No Abstract] [Full Text] [Related]
15. [Study of CATCH 22: genetic aspects].
Antonenko VG; Ivanov VI; Konstantinova LM; Levina LIa; Mglinets VA
Vestn Ross Akad Med Nauk; 2000; (5):46-50. PubMed ID: 10881663
[TBL] [Abstract][Full Text] [Related]
16. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
Wulfsberg EA
Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634
[No Abstract] [Full Text] [Related]
17. 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]
18. [Relationship between 22q11 microdeletion syndrome and congenital heart disease].
Qin YF; Xie CH; Yang JB; Wu DW; Shao J; Zhao ZY
Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Jul; 39(7):631-5. PubMed ID: 22088244
[TBL] [Abstract][Full Text] [Related]
19. CATCH22 syndrome with gastroesophageal reflux.
Osaki Y; Oana S; Yasukawa K; Fujimori K; Terai M; Niimi H
Pediatr Int; 2000 Aug; 42(4):367-8. PubMed ID: 10986867
[No Abstract] [Full Text] [Related]
20. Kousseff syndrome caused by deletion of chromosome 22q11-13.
Forrester S; Kovach MJ; Smith RE; Rimer L; Wesson M; Kimonis VE
Am J Med Genet; 2002 Nov; 112(4):338-42. PubMed ID: 12376934
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]