PubMed (OMIM) for id: 65085

Year	Number of Results
1981	1
1984	1
1985	3
1986	2
1987	1
1991	1
1992	4
1993	2
1994	2
1995	4
1996	1
1997	7
1998	1
1999	4
2000	2
2001	13
2002	6
2003	5
2006	1
2024	0

1

Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.

Guris DL, Duester G, Papaioannou VE, Imamoto A. Guris DL, et al. Dev Cell. 2006 Jan;10(1):81-92. doi: 10.1016/j.devcel.2005.12.002. Dev Cell. 2006. PMID: 16399080 Free article.

2

Role of TBX1 in human del22q11.2 syndrome.

Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, Ichida F, Joo K, Kimura M, Imamura S, Kamatani N, Momma K, Takao A, Nakazawa M, Shimizu N, Matsuoka R. Yagi H, et al. Lancet. 2003 Oct 25;362(9393):1366-73. doi: 10.1016/s0140-6736(03)14632-6. Lancet. 2003. PMID: 14585638

3

No justification of routine screening for 22q11 deletions in patients with overt cleft palate.

Ruiter EM, Bongers EM, Smeets D, Kuijpers-Jagtman AM, Hamel BC. Ruiter EM, et al. Clin Genet. 2003 Sep;64(3):216-9. doi: 10.1034/j.1399-0004.2003.00134.x. Clin Genet. 2003. PMID: 12919136

4

TBX1 is required for inner ear morphogenesis.

Vitelli F, Viola A, Morishima M, Pramparo T, Baldini A, Lindsay E. Vitelli F, et al. Hum Mol Genet. 2003 Aug 15;12(16):2041-8. doi: 10.1093/hmg/ddg216. Hum Mol Genet. 2003. PMID: 12913075

5

T-box genes in human disorders.

Packham EA, Brook JD. Packham EA, et al. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R37-44. doi: 10.1093/hmg/ddg077. Hum Mol Genet. 2003. PMID: 12668595 Review.

6

VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

Stalmans I, Lambrechts D, De Smet F, Jansen S, Wang J, Maity S, Kneer P, von der Ohe M, Swillen A, Maes C, Gewillig M, Molin DG, Hellings P, Boetel T, Haardt M, Compernolle V, Dewerchin M, Plaisance S, Vlietinck R, Emanuel B, Gittenberger-de Groot AC, Scambler P, Morrow B, Driscol DA, Moons L, Esguerra CV, Carmeliet G, Behn-Krappa A, Devriendt K, Collen D, Conway SJ, Carmeliet P. Stalmans I, et al. Nat Med. 2003 Feb;9(2):173-82. doi: 10.1038/nm819. Epub 2003 Jan 21. Nat Med. 2003. PMID: 12539040

7

Pulmonary agenesis: expansion of the VCFS phenotype.

Conway K, Gibson R, Perkins J, Cunningham ML. Conway K, et al. Am J Med Genet. 2002 Nov 15;113(1):89-92. doi: 10.1002/ajmg.10673. Am J Med Genet. 2002. PMID: 12400071

8

Kousseff syndrome caused by deletion of chromosome 22q11-13.

Forrester S, Kovach MJ, Smith RE, Rimer L, Wesson M, Kimonis VE. Forrester S, et al. Am J Med Genet. 2002 Nov 1;112(4):338-42. doi: 10.1002/ajmg.10625. Am J Med Genet. 2002. PMID: 12376934

9

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

Baldini A. Baldini A. Hum Mol Genet. 2002 Oct 1;11(20):2363-9. doi: 10.1093/hmg/11.20.2363. Hum Mol Genet. 2002. PMID: 12351571 Review.

10

Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome.

Sandrin-Garcia P, Macedo C, Martelli LR, Ramos ES, Guion-Almeida ML, Richieri-Costa A, Passos GA. Sandrin-Garcia P, et al. Clin Genet. 2002 May;61(5):380-3. doi: 10.1034/j.1399-0004.2002.610511.x. Clin Genet. 2002. PMID: 12081724

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