893 related articles for article (PubMed ID: 9216164)
1. 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]
2. 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]
3. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.
Lindsay EA; Greenberg F; Shaffer LG; Shapira SK; Scambler PJ; Baldini A
Am J Med Genet; 1995 Mar; 56(2):191-7. PubMed ID: 7625444
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
Goldmuntz E; Driscoll D; Budarf ML; Zackai EH; McDonald-McGinn DM; Biegel JA; Emanuel BS
J Med Genet; 1993 Oct; 30(10):807-12. PubMed ID: 7901419
[TBL] [Abstract][Full Text] [Related]
6. Clinical correlation of chromosome 22q11.2 fluorescent in situ hybridization analysis and velocardiofacial syndrome.
Oh AK; Workman LA; Wong GB
Cleft Palate Craniofac J; 2007 Jan; 44(1):62-6. PubMed ID: 17214538
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes.
Cuneo BF
Curr Opin Pediatr; 2001 Oct; 13(5):465-72. PubMed ID: 11801894
[TBL] [Abstract][Full Text] [Related]
10. Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.
Takahashi K; Kido S; Hoshino K; Ogawa K; Ohashi H; Fukushima Y
Eur J Pediatr; 1995 Nov; 154(11):878-81. PubMed ID: 8582397
[TBL] [Abstract][Full Text] [Related]
11. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
Brunet A; Gabau E; Perich RM; Valdesoiro L; Brun C; Caballín MR; Guitart M
Am J Med Genet A; 2006 Nov; 140(22):2426-32. PubMed ID: 17041934
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
Driscoll DA; Salvin J; Sellinger B; Budarf ML; McDonald-McGinn DM; Zackai EH; Emanuel BS
J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.
McDonald-McGinn DM; Driscoll DA; Emanuel BS; Goldmuntz E; Clark BJ; Solot C; Cohen M; Schultz P; LaRossa D; Randall P; Zackai EH
Pediatrics; 1997 May; 99(5):E9. PubMed ID: 9113966
[TBL] [Abstract][Full Text] [Related]
19. The deletions of 22q11--the Portuguese experience.
Gaspar IM; Lourenço MT; Reis MI; Soares MA; Nogueira G; Ferreira F; Feijóo MJ
Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]