389 related articles for article (PubMed ID: 12210289)
1. Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome.
Bearden CE; Wang PP; Simon TJ
Am J Med Genet; 2002 Aug; 114(6):689-92. PubMed ID: 12210289
[No Abstract] [Full Text] [Related]
2. 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]
3. [Transient neonatal hypocalcemia. Onset Manifestation of the 22q11.2 deletion syndrome].
Pusceddu M; Bertone A; Campra D; Pontoriero D; Guala A
Minerva Pediatr; 2002 Aug; 54(4):343-5. PubMed ID: 12131871
[No Abstract] [Full Text] [Related]
4. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome].
Hjalgrim H; Hahnemann JM; Timshel S; Brøndum-Nielsen K
Ugeskr Laeger; 2000 Jul; 162(31):4169-70. PubMed ID: 10962926
[No Abstract] [Full Text] [Related]
5. A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?
Henwood J; Pickard C; Leek JP; Bennett CP; Crow YJ; Thompson JD; Ahmed M; Watterson KG; Parsons JM; Roberts E; Lench NJ
J Med Genet; 2001 Aug; 38(8):533-6. PubMed ID: 11494964
[No Abstract] [Full Text] [Related]
6. Altered replication timing of the HIRA/Tuple1 locus in the DiGeorge and Velocardiofacial syndromes.
D'Antoni S; Mattina T; Di Mare P; Federico C; Motta S; Saccone S
Gene; 2004 May; 333():111-9. PubMed ID: 15177686
[TBL] [Abstract][Full Text] [Related]
7. [DiGeorge syndrome. Velocardiofacial syndrome/chromosome 22q11 deletion syndrome].
Hoffmann MH; Vadstrup S
Ugeskr Laeger; 2000 May; 162(19):2736-9. PubMed ID: 10827540
[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. What's in a name? Chromosome 22q abnormalities and the DiGeorge, velocardiofacial, and conotruncal anomalies face syndromes.
Wulfsberg EA; Leana-Cox J; Neri G
Am J Med Genet; 1996 Nov; 65(4):317-9. PubMed ID: 8923942
[No Abstract] [Full Text] [Related]
10. Genetic basis of DiGeorge and velocardiofacial syndromes.
Driscoll DA
Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818
[TBL] [Abstract][Full Text] [Related]
11. Avoiding perils and pitfalls in velocardiofacial syndrome: an otolaryngologist's perspective.
Cable BB; Mair EA
Ear Nose Throat J; 2003 Jan; 82(1):56-60. PubMed ID: 12610907
[TBL] [Abstract][Full Text] [Related]
12. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.
Marino B; Digilio MC; Toscano A; Giannotti A; Dallapiccola B
Genet Couns; 1999; 10(1):25-33. PubMed ID: 10191426
[TBL] [Abstract][Full Text] [Related]
13. [DiGeorge syndrome. An underdiagnosed disease category with different clinical features].
Graesdal A; Surén P; Vadstrup S
Tidsskr Nor Laegeforen; 2001 Nov; 121(27):3177-9. PubMed ID: 11876140
[TBL] [Abstract][Full Text] [Related]
14. Velocardiofacial syndrome and DiGeorge sequence.
Shprintzen RJ
J Med Genet; 1994 May; 31(5):423-4. PubMed ID: 8064827
[No Abstract] [Full Text] [Related]
15. Velocardiofacial syndrome presenting as hypocalcemia in early adolescence.
Sykes KS; Bachrach LK; Siegel-Bartelt J; Ipp M; Kooh SW; Cytrynbaum C
Arch Pediatr Adolesc Med; 1997 Jul; 151(7):745-7. PubMed ID: 9232055
[No Abstract] [Full Text] [Related]
16. Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).
Perez E; Sullivan KE
Curr Opin Pediatr; 2002 Dec; 14(6):678-83. PubMed ID: 12436034
[TBL] [Abstract][Full Text] [Related]
17. [CATCH 22].
Matsuo N; Yamagishi H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):150-3. PubMed ID: 11057175
[No Abstract] [Full Text] [Related]
18. Noncompaction is already known in DiGeorge anomaly from 22q11.2 deletion.
Stöllberger C; Finsterer J
Am J Med Genet A; 2011 Mar; 155A(3):662-3; author reply 664-5. PubMed ID: 21337687
[No Abstract] [Full Text] [Related]
19. A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
Zarchi O; Attias J; Raveh E; Basel-Vanagaite L; Saporta L; Gothelf D
J Pediatr; 2011 Feb; 158(2):301-6. PubMed ID: 20846670
[TBL] [Abstract][Full Text] [Related]
20. Multiple congenital anomalies, thymic dysplasia, severe congenital heart disease, and oligosyndactyly with a deletion of the short arm of chromosome 5.
Taylor MJ; Josifek K
Am J Med Genet; 1981; 9(1):5-11. PubMed ID: 6264787
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]