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Results: 16

Related Articles by Review for PubMed (Select 22185286)

1.

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.

Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, Sun HJ, Bao LM, Shen J, Fu QH, Li F, Sun K.

BMC Med Genet. 2011 Dec 21;12:169. doi: 10.1186/1471-2350-12-169.

2.

Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome.

Momma K.

Am J Cardiol. 2010 Jun 1;105(11):1617-24. doi: 10.1016/j.amjcard.2010.01.333. Review.

PMID:
20494672
3.

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
4.

Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.

Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen WL, Wang W.

Gene. 2013 Sep 15;527(1):405-9. doi: 10.1016/j.gene.2013.06.009. Epub 2013 Jun 17. Review.

PMID:
23791650
5.

22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.

Scambler PJ.

Pediatr Cardiol. 2010 Apr;31(3):378-90. doi: 10.1007/s00246-009-9613-0. Review.

PMID:
20054531
6.

CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.

Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.

Pathologica. 1999 Jun;91(3):166-72. Review.

PMID:
10536461
7.

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. Review.

PMID:
10191426
8.

Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.

Gao S, Li X, Amendt BA.

Curr Allergy Asthma Rep. 2013 Dec;13(6):613-21. doi: 10.1007/s11882-013-0384-6. Review.

9.

A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review.

Fernández L, Nevado J, Santos F, Heine-Suñer D, Martinez-Glez V, García-Miñaur S, Palomo R, Delicado A, Pajares IL, Palomares M, García-Guereta L, Valverde E, Hawkins F, Lapunzina P.

BMC Med Genet. 2009 Jun 2;10:48. doi: 10.1186/1471-2350-10-48. Review.

10.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
11.

Genetic basis of DiGeorge and velocardiofacial syndromes.

Driscoll DA.

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

PMID:
7849818
12.

Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome.

Aggarwal VS, Morrow BE.

Dev Disabil Res Rev. 2008;14(1):19-25. doi: 10.1002/ddrr.4. Review.

13.

Heart defects and other features of the 22q11 distal deletion syndrome.

Fagerberg CR, Graakjaer J, Heinl UD, Ousager LB, Dreyer I, Kirchhoff M, Rasmussen AA, Lautrup CK, Birkebaek N, Sorensen K.

Eur J Med Genet. 2013 Feb;56(2):98-107. doi: 10.1016/j.ejmg.2012.09.009. Epub 2012 Oct 10. Review.

PMID:
23063575
14.

Tetralogy of Fallot with complete DiGeorge syndrome: report of a case and a review of the literature.

Kobayashi D, Sallaam S, Humes RA.

Congenit Heart Dis. 2013 Jul-Aug;8(4):E119-26. doi: 10.1111/j.1747-0803.2012.00694.x. Epub 2012 Aug 7. Review.

PMID:
22883347
15.

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.

Kobrynski LJ, Sullivan KE.

Lancet. 2007 Oct 20;370(9596):1443-52. Review.

PMID:
17950858
16.

22q11 deletion syndrome: current perspective.

Hacıhamdioğlu B, Hacıhamdioğlu D, Delil K.

Appl Clin Genet. 2015 May 18;8:123-32. doi: 10.2147/TACG.S82105. eCollection 2015. Review.

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