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Items: 1 to 20 of 49

1.

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden.

Oskarsdóttir S, Vujic M, Fasth A.

Arch Dis Child. 2004 Feb;89(2):148-51.

2.

The 22q11.2 deletion syndrome.

Yamagishi H.

Keio J Med. 2002 Jun;51(2):77-88. Review.

3.

Genetic basis of DiGeorge and velocardiofacial syndromes.

Driscoll DA.

Curr Opin Pediatr. 1994 Dec;6(6):702-6. Review.

PMID:
7849818
4.

22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes.

Cuneo BF.

Curr Opin Pediatr. 2001 Oct;13(5):465-72. Review. Erratum in: Curr Opin Pediatr 2002 Apr;14(2):286.

PMID:
11801894
5.

Velo-cardio-facial syndrome: 30 Years of study.

Shprintzen RJ.

Dev Disabil Res Rev. 2008;14(1):3-10. doi: 10.1002/ddrr.2. Review.

6.

Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).

Perez E, Sullivan KE.

Curr Opin Pediatr. 2002 Dec;14(6):678-83. Review.

PMID:
12436034
7.

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.

Arinami T.

J Hum Genet. 2006;51(12):1037-45. Epub 2006 Sep 13. Review.

PMID:
16969581
8.

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

Portnoï MF, Lebas F, Gruchy N, Ardalan A, Biran-Mucignat V, Malan V, Finkel L, Roger G, Ducrocq S, Gold F, Taillemite JL, Marlin S.

Am J Med Genet A. 2005 Aug 15;137(1):47-51. Review.

PMID:
16007629
9.

[Schizophrenia and the 22q11 deletion syndrome].

Güzelcan Y, van Amelsvoort T, de Haan L, van Schaik P, Linszen DH.

Ned Tijdschr Geneeskd. 2002 Oct 26;146(43):2019-21. Review. Dutch.

PMID:
12428460
10.

Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.

De Smedt B, Swillen A, Verschaffel L, Ghesquière P.

Dev Disabil Res Rev. 2009;15(1):4-10. doi: 10.1002/ddrr.44. Review.

PMID:
19213009
11.

The 22q11.2 deletion syndrome.

Emanuel BS, McDonald-McGinn D, Saitta SC, Zackai EH.

Adv Pediatr. 2001;48:39-73. Review.

PMID:
11480765
12.

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 11;65(4):309-16. Review.

PMID:
8923941
13.

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

McDonald-McGinn DM, Sullivan KE.

Medicine (Baltimore). 2011 Jan;90(1):1-18. doi: 10.1097/MD.0b013e3182060469. Review.

14.

When half is not enough: gene expression and dosage in the 22q11 deletion syndrome.

Meechan DW, Maynard TM, Gopalakrishna D, Wu Y, LaMantia AS.

Gene Expr. 2007;13(6):299-310. Review.

PMID:
17708416
15.

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. doi: 10.1002/ddrr.6. Review.

PMID:
18636635
16.

DiGeorge syndrome: new insights.

Goldmuntz E.

Clin Perinatol. 2005 Dec;32(4):963-78, ix-x. Review.

PMID:
16325672
17.

[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].

Demily C, Rossi M, Schneider M, Edery P, Leleu A, d'Amato T, Franck N, Eliez S.

Encephale. 2015 Jun;41(3):266-73. doi: 10.1016/j.encep.2014.10.005. Epub 2014 Dec 16. Review. French.

PMID:
25523123
18.

Velo-cardio-facial syndrome.

Shprintzen RJ, Higgins AM, Antshel K, Fremont W, Roizen N, Kates W.

Curr Opin Pediatr. 2005 Dec;17(6):725-30. Review.

PMID:
16282778
19.

DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome.

Sullivan KE.

Adv Exp Med Biol. 2007;601:37-49. Review.

PMID:
17712990
20.

Hypocalcemia and chromosome 22q11 microdeletion.

Garabédian M.

Genet Couns. 1999;10(4):389-94. Review.

PMID:
10631928
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