573 related articles for article (PubMed ID: 18424337)
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. Genetic compensation in a human genomic disorder.
Carelle-Calmels N; Saugier-Veber P; Girard-Lemaire F; Rudolf G; Doray B; Guérin E; Kuhn P; Arrivé M; Gilch C; Schmitt E; Fehrenbach S; Schnebelen A; Frébourg T; Flori E
N Engl J Med; 2009 Mar; 360(12):1211-6. PubMed ID: 19297573
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
Carotti A; Digilio MC; Piacentini G; Saffirio C; Di Donato RM; Marino B
Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
[TBL] [Abstract][Full Text] [Related]
25. [CATCH22 or 22q11 deletion syndrome. An underdiagnosed and misunderstood disease category with a variable clinical picture].
Oskarsdóttir S; Fasth A; Belfrage M; Viggedal G; Persson C; Eriksson BO
Lakartidningen; 1999 Nov; 96(44):4789-93. PubMed ID: 10584540
[TBL] [Abstract][Full Text] [Related]
26. [22q11.2 deletion syndrome].
Ishikawa T
Nihon Rinsho; 2006 Jun; Suppl 2():70-3. PubMed ID: 16817353
[No Abstract] [Full Text] [Related]
27. Deletion of chromosome 22q11 and pseudohypoparathyroidism.
Craigen WJ; Lindsay EA; Bricker JT; Hawkins EP; Baldini A
Am J Med Genet; 1997 Oct; 72(1):63-5. PubMed ID: 9295077
[TBL] [Abstract][Full Text] [Related]
28. Possible mechanisms and gene involvement in speech problems in the 22q11.2 deletion syndrome.
Widdershoven JC; Beemer FA; Kon M; Dejonckere PH; Mink van der Molen AB
J Plast Reconstr Aesthet Surg; 2008 Sep; 61(9):1016-23. PubMed ID: 18554997
[TBL] [Abstract][Full Text] [Related]
29. Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome.
Lawrence S; McDonald-McGinn DM; Zackai E; Sullivan KE
J Pediatr; 2003 Aug; 143(2):277-8. PubMed ID: 12970648
[TBL] [Abstract][Full Text] [Related]
30. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
Qin YF; Yang JB; Xie CH; Shao J; Zhao ZY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
[TBL] [Abstract][Full Text] [Related]
31. [Epilepsy in an adult with chromosome 22q11 micro-deletion].
Alla P; Philip N; Azulay JP; Attarian S; Pouget J
Rev Neurol (Paris); 1999 Nov; 155(11):967-70. PubMed ID: 10603642
[TBL] [Abstract][Full Text] [Related]
32. Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
McDonald-McGinn DM; Sullivan KE
Medicine (Baltimore); 2011 Jan; 90(1):1-18. PubMed ID: 21200182
[TBL] [Abstract][Full Text] [Related]
33. The 22q11.2 deletion syndrome: more answers but more questions.
Fernhoff PM
J Pediatr; 2000 Aug; 137(2):145-7. PubMed ID: 10931401
[No Abstract] [Full Text] [Related]
34. [DiGeorge syndrome, a review of 52 patients].
Minier F; Carles D; Pelluard F; Alberti EM; Stern L; Saura R
Arch Pediatr; 2005 Mar; 12(3):254-7. PubMed ID: 15734119
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. [Diagnosis of 22q11.2 deletion syndrome in the context of newly developed psychosis].
Kaltenboeck A; Friedrich F; Hinterbuchinger B; Litvan Z; Mossaheb N
Neuropsychiatr; 2016 Dec; 30(4):223-226. PubMed ID: 27822729
[TBL] [Abstract][Full Text] [Related]
37. Annotation: velo-cardio-facial syndrome.
Murphy KC
J Child Psychol Psychiatry; 2005 Jun; 46(6):563-71. PubMed ID: 15877762
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome.
Driscoll DA
Methods Mol Med; 2006; 126():43-55. PubMed ID: 16930005
[TBL] [Abstract][Full Text] [Related]
40. Concurrent microdeletion and duplication of 22q11.2.
Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]