181 related articles for article (PubMed ID: 12955254)
21. [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]
22. Velopharyngeal, speech and dental characteristics as diagnostic aids in 22q11.2 deletion syndrome.
Oberoi S; Huynh L; Vargervik K
J Calif Dent Assoc; 2011 May; 39(5):327-32. PubMed ID: 21721477
[TBL] [Abstract][Full Text] [Related]
23. Palatal evaluation and treatment in 22q11.2 deletion syndrome.
Jackson O; Crowley TB; Sharkus R; Smith R; Jeong S; Solot C; McDonald-Mcginn D
Am J Med Genet A; 2019 Jul; 179(7):1184-1195. PubMed ID: 31038278
[TBL] [Abstract][Full Text] [Related]
24. Cognitive and language issues associated with cleft lip and palate.
Hardin-Jones M; Chapman KL
Semin Speech Lang; 2011 May; 32(2):127-40. PubMed ID: 21948639
[TBL] [Abstract][Full Text] [Related]
25. [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]
26. Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.
Schindewolf E; Khalek N; Johnson MP; Gebb J; Coleman B; Crowley TB; Zackai EH; McDonald-McGinn DM; Moldenhauer JS
Am J Med Genet A; 2018 Aug; 176(8):1735-1741. PubMed ID: 30055034
[TBL] [Abstract][Full Text] [Related]
27. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
28. DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome.
Sullivan KE
Adv Exp Med Biol; 2007; 601():37-49. PubMed ID: 17712990
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. [ORL and speech aspects in DiGeorge syndrome].
Portmann D; Marraco M; Lacombe D; Taine L; Gadan C; Siberchicot F
Rev Laryngol Otol Rhinol (Bord); 1997; 118(4):273-8. PubMed ID: 9637100
[TBL] [Abstract][Full Text] [Related]
31. Surgical considerations in 22Q11.2 deletion syndrome.
Kirschner RE; Baylis AL
Clin Plast Surg; 2014 Apr; 41(2):271-82. PubMed ID: 24607194
[TBL] [Abstract][Full Text] [Related]
32. Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature.
Leana-Cox J; Pangkanon S; Eanet KR; Curtin MS; Wulfsberg EA
Am J Med Genet; 1996 Nov; 65(4):309-16. PubMed ID: 8923941
[TBL] [Abstract][Full Text] [Related]
33. 22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate.
Carpeta S; Pineda T; Martínez MC; Osorio G; Porras-Hurtado GL; Rojas J; Zarante I; Moreno-Niño OM
Cleft Palate Craniofac J; 2019 Jan; 56(1):116-122. PubMed ID: 29652534
[TBL] [Abstract][Full Text] [Related]
34. Ocular findings in children with a microdeletion in chromosome 22q11.2.
Casteels I; Casaer P; Gewillig M; Swillen A; Devriendt K
Eur J Pediatr; 2008 Jul; 167(7):751-5. PubMed ID: 17704945
[TBL] [Abstract][Full Text] [Related]
35. A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.
Widdershoven JC; Bowser M; Sheridan MB; McDonald-McGinn DM; Zackai EH; Solot CB; Kirschner RE; Beemer FA; Morrow BE; Devoto M; Emanuel BS
Int J Pediatr Otorhinolaryngol; 2013 Jan; 77(1):123-7. PubMed ID: 23121717
[TBL] [Abstract][Full Text] [Related]
36. Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia.
Cuturilo G; Drakulic D; Jovanovic I; Krstic A; Djukic M; Skoric D; Mijovic M; Stefanovic I; Milivojevic M; Stevanovic M
Indian Pediatr; 2016 Sep; 53(9):786-789. PubMed ID: 27771646
[TBL] [Abstract][Full Text] [Related]
37. Superiorly based pharyngeal flap for treatment of velopharyngeal insufficiency in patients with 22q11.2 deletion syndrome.
Filip C; Matzen M; Aukner R; Moe M; Høgevold HE; Åbyholm F; Abrahamsen TG; Tønseth K
J Craniofac Surg; 2013 Mar; 24(2):501-4. PubMed ID: 23524725
[TBL] [Abstract][Full Text] [Related]
38. Labyrinthine malformation in the 22q11.2 deletion syndrome.
Hopsu E; Markkola A; Pitkäranta A
Clin Dysmorphol; 2007 Jan; 16(1):67-68. PubMed ID: 17159521
[TBL] [Abstract][Full Text] [Related]
39. Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome.
Lay-Son G; Palomares M; Guzman ML; Vasquez M; Puga A; Repetto GM
Int J Pediatr Otorhinolaryngol; 2012 Dec; 76(12):1726-8. PubMed ID: 22939891
[TBL] [Abstract][Full Text] [Related]
40. [Clinical case of congenital cleft palate in 22q11.2 deletion syndrome].
Ginter OV; Namazova-Baranova LS; Mospan TY; Jourkova NV; Davydova IV; Pushkov AA
Stomatologiia (Mosk); 2019; 98(1):61-63. PubMed ID: 30830095
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]