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Items: 1 to 20 of 25

1.

The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.

Piotrowski T, Ahn DG, Schilling TF, Nair S, Ruvinsky I, Geisler R, Rauch GJ, Haffter P, Zon LI, Zhou Y, Foott H, Dawid IB, Ho RK.

Development. 2003 Oct;130(20):5043-52.

2.

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
3.

DiGeorge syndrome: an update.

Baldini A.

Curr Opin Cardiol. 2004 May;19(3):201-4. Review.

PMID:
15096950
4.

Dissecting contiguous gene defects: TBX1.

Baldini A.

Curr Opin Genet Dev. 2005 Jun;15(3):279-84. Review.

PMID:
15917203
5.

Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.

Stalmans I.

Verh K Acad Geneeskd Belg. 2005;67(4):229-76. Review.

PMID:
16334858
6.

T-box genes in human disorders.

Packham EA, Brook JD.

Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R37-44. Review.

7.

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.

8.

DiGeorge syndrome: the use of model organisms to dissect complex genetics.

Baldini A.

Hum Mol Genet. 2002 Oct 1;11(20):2363-9. Review.

9.

Developing models of DiGeorge syndrome.

Epstein JA.

Trends Genet. 2001 Oct;17(10):S13-7. Review.

PMID:
11585671
10.

Mouse models of 22q11 deletion syndrome.

Paylor R, Lindsay E.

Biol Psychiatry. 2006 Jun 15;59(12):1172-9. Epub 2006 Apr 17. Review.

PMID:
16616724
11.

22q11 deletion syndrome: a review of some developmental biology aspects of the cardiovascular system.

Restivo A, Sarkozy A, Digilio MC, Dallapiccola B, Marino B.

J Cardiovasc Med (Hagerstown). 2006 Feb;7(2):77-85. Review.

PMID:
16645366
12.

Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome.

Yamagishi H, Srivastava D.

Trends Mol Med. 2003 Sep;9(9):383-9. Review.

PMID:
13129704
13.

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
14.

DiGeorge syndrome and pharyngeal apparatus development.

Wurdak H, Ittner LM, Sommer L.

Bioessays. 2006 Nov;28(11):1078-86. Review.

PMID:
17041894
15.

The role of the endoderm in the development and evolution of the pharyngeal arches.

Graham A, Okabe M, Quinlan R.

J Anat. 2005 Nov;207(5):479-87. Review.

16.

Understanding velocardiofacial syndrome: how recent discoveries can help you improve your patient outcomes.

Chinnadurai S, Goudy S.

Curr Opin Otolaryngol Head Neck Surg. 2012 Dec;20(6):502-6. doi: 10.1097/MOO.0b013e328359b476. Review.

PMID:
23000736
17.

Neural crest migration and mouse models of congenital heart disease.

Gitler AD, Brown CB, Kochilas L, Li J, Epstein JA.

Cold Spring Harb Symp Quant Biol. 2002;67:57-62. Review. No abstract available.

PMID:
12858524
18.

[Molecular mechanism of thymus development in the pharyngeal arch].

Okubo T, Takada S.

Seikagaku. 2012 Mar;84(3):168-76. Review. Japanese. No abstract available.

PMID:
22568068
19.

Craniofacial development: the tissue and molecular interactions that control development of the head.

Francis-West PH, Robson L, Evans DJ.

Adv Anat Embryol Cell Biol. 2003;169:III-VI, 1-138. Review.

PMID:
12793205
20.

Development of the pharyngeal arches.

Graham A.

Am J Med Genet A. 2003 Jun 15;119A(3):251-6. Review.

PMID:
12784288
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