336 related articles for article (PubMed ID: 18636630)
1. Introduction: advances in research on velo-cardio-facial syndrome/22q11.2 deletion syndrome.
Kates WR; Emanuel BS
Dev Disabil Res Rev; 2008; 14(1):1-2. PubMed ID: 18636630
[No Abstract] [Full Text] [Related]
2. Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region.
Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
Eur J Pediatr Surg; 1993 Dec; 3 Suppl 1():27-8. PubMed ID: 8130147
[No Abstract] [Full Text] [Related]
3. [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]
4. [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]
5. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Sullivan KE
Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
[TBL] [Abstract][Full Text] [Related]
6. Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Gothelf D; Schaer M; Eliez S
Dev Disabil Res Rev; 2008; 14(1):59-68. PubMed ID: 18636637
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome).
Digilio MC; Giannotti A; Castro M; Colistro F; Ferretti F; Marino B; Dallapiccola B
Am J Med Genet A; 2003 Sep; 121A(3):286-8. PubMed ID: 12923874
[No Abstract] [Full Text] [Related]
9. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
Funke B; Pandita RK; Morrow BE
Genomics; 2001 May; 73(3):264-71. PubMed ID: 11350118
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. The neurocognitive phenotype in velo-cardio-facial syndrome: a developmental perspective.
Antshel KM; Fremont W; Kates WR
Dev Disabil Res Rev; 2008; 14(1):43-51. PubMed ID: 18636636
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study.
Schaer M; Schmitt JE; Glaser B; Lazeyras F; Delavelle J; Eliez S
Psychiatry Res; 2006 Jan; 146(1):1-11. PubMed ID: 16388934
[TBL] [Abstract][Full Text] [Related]
14. [Chromosome 22q11 and schizophrenia].
Agatsuma S; Hiroi N
Nihon Shinkei Seishin Yakurigaku Zasshi; 2005 Apr; 25(2):79-84. PubMed ID: 16220657
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Phenotypic variability: genetics and chance--deletion 22q11 and schizophrenia].
Breuning MH
Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2016-9. PubMed ID: 12428459
[TBL] [Abstract][Full Text] [Related]
17. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
Staple L; Andrews T; McDonald-McGinn D; Zackai E; Sullivan KE
Pediatr Allergy Immunol; 2005 May; 16(3):226-30. PubMed ID: 15853951
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Deletion 22q11: spectrum of associated disorders.
Hay BN
Semin Pediatr Neurol; 2007 Sep; 14(3):136-9. PubMed ID: 17980310
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
