457 related articles for article (PubMed ID: 11006712)
1. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
Morava E; Masszi G; Czakó M; Tóth G; Melegh B; Kosztolányi G
Orv Hetil; 2000 Aug; 141(34):1873-5. PubMed ID: 11006712
[TBL] [Abstract][Full Text] [Related]
2. Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Vantrappen G; Devriendt K; Swillen A; Rommel N; Vogels A; Eyskens B; Gewillig M; Feenstra L; Fryns JP
Genet Couns; 1999; 10(1):3-9. PubMed ID: 10191424
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.
Vantrappen G; Rommel N; Swillen A; Cremers CW; Fryns JP; Devriendt K
Acta Otorhinolaryngol Belg; 2003; 57(2):101-6. PubMed ID: 12836465
[TBL] [Abstract][Full Text] [Related]
5. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
Frohn-Mulder IM; Wesby Swaay E; Bouwhuis C; Van Hemel JO; Gerritsma E; Niermeyer MF; Hess J
Genet Couns; 1999; 10(1):35-41. PubMed ID: 10191427
[TBL] [Abstract][Full Text] [Related]
6. Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome.
Rommel N; Vantrappen G; Swillen A; Devriendt K; Feenstra L; Fryns JP
Genet Couns; 1999; 10(1):71-8. PubMed ID: 10191432
[TBL] [Abstract][Full Text] [Related]
7. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Fragile X syndrome and 22q11.2 microdeletion in the same sibship.
Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N
Am J Med Genet; 2000 Dec; 95(4):358-60. PubMed ID: 11186890
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. [Syndromes 3. Velo-cardio-facial (VCF/Shprintzen) syndrome].
Beemer FA
Ned Tijdschr Tandheelkd; 1998 Aug; 105(8):287-8. PubMed ID: 11928434
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [Cerebral polymicrogyria and 22q11 deletion syndrome].
Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Shprintzen (velo-cardio-facial) syndrome: a rare case.
Alkan T; Akçevin A; Türkoglu H; Paker T; Aytaç A
ASAIO J; 2006; 52(6):e33-4. PubMed ID: 17117043
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
