108 related articles for article (PubMed ID: 8773902)
1. The search for hemizygosity at 22qll in patients with isolated cleft palate.
Mingarelli R; Digilio MC; Mari A; Amati F; Standoli L; Giannotti A; Novelli G; Dallapiccola B
J Craniofac Genet Dev Biol; 1996; 16(2):118-21. PubMed ID: 8773902
[TBL] [Abstract][Full Text] [Related]
2. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A
Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167
[TBL] [Abstract][Full Text] [Related]
3. Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.
Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
Am J Med Genet; 1994 Oct; 52(4):445-9. PubMed ID: 7747757
[TBL] [Abstract][Full Text] [Related]
4. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.
Driscoll DA; Spinner NB; Budarf ML; McDonald-McGinn DM; Zackai EH; Goldberg RB; Shprintzen RJ; Saal HM; Zonana J; Jones MC
Am J Med Genet; 1992 Sep; 44(2):261-8. PubMed ID: 1360769
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Search for deletion 22q11.2 in interphase nuclei of buccal mucosa of patients ascertained by isolated cleft palate: a new diagnostic approach.
Shouman N; Pabst B; Arslan-Kirchner M; Eckardt A; Schönweiler R; Ptok M; Mehraein Y; Schmidtke J; Miller K
Int J Oral Maxillofac Surg; 2003 Apr; 32(2):198-200. PubMed ID: 12729782
[TBL] [Abstract][Full Text] [Related]
8. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
Kelly D; Goldberg R; Wilson D; Lindsay E; Carey A; Goodship J; Burn J; Cross I; Shprintzen RJ; Scambler PJ
Am J Med Genet; 1993 Feb; 45(3):308-12. PubMed ID: 8434616
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2.
Li M; Zackai EH; Niikawa N; Kaplan P; Driscoll DA
Am J Med Genet; 1996 Oct; 65(2):101-3. PubMed ID: 8911598
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Is isolated palatal anomaly an indication to screen for 22q11 region deletion?
Reish O; Finkelstein Y; Mesterman R; Nachmani A; Wolach B; Fejgin M; Amiel A
Cleft Palate Craniofac J; 2003 Mar; 40(2):176-9. PubMed ID: 12605524
[TBL] [Abstract][Full Text] [Related]
14. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
Ford LC; Sulprizio SL; Rasgon BM
Laryngoscope; 2000 Mar; 110(3 Pt 1):362-7. PubMed ID: 10718420
[TBL] [Abstract][Full Text] [Related]
15. Velocardiofacial manifestations and microdeletions in schizophrenic inpatients.
Gothelf D; Frisch A; Munitz H; Rockah R; Aviram A; Mozes T; Birger M; Weizman A; Frydman M
Am J Med Genet; 1997 Nov; 72(4):455-61. PubMed ID: 9375731
[TBL] [Abstract][Full Text] [Related]
16. 22q11 Deletion in children with cleft lip and palate--is routine screening justified?
Bashir MA; Hodgkinson PD; Montgomery T; Splitt M
J Plast Reconstr Aesthet Surg; 2008; 61(2):130-2. PubMed ID: 17707704
[TBL] [Abstract][Full Text] [Related]
17. [Sensitivity and specificity of endoscopy for the detection of velocardiofacial syndrome].
Ysunza A; Pamplona M; Silva-Rojas A; Mazón JJ; Ramírez E; Canún S; Sierra Mdel C; Cervantes A
Rev Invest Clin; 2004; 56(4):454-9. PubMed ID: 15587291
[TBL] [Abstract][Full Text] [Related]
18. Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch.
Rauch A; Hofbeck M; Leipold G; Klinge J; Trautmann U; Kirsch M; Singer H; Pfeiffer RA
Am J Med Genet; 1998 Jul; 78(4):322-31. PubMed ID: 9714433
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency.
Zori RT; Boyar FZ; Williams WN; Gray BA; Bent-Williams A; Stalker HJ; Rimer LA; Nackashi JA; Driscoll DJ; Rasmussen SA; Dixon-Wood V; Williams CA
Am J Med Genet; 1998 Apr; 77(1):8-11. PubMed ID: 9557885
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]