Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 8

1.

Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors.

Chmielecki J, Crago AM, Rosenberg M, O'Connor R, Walker SR, Ambrogio L, Auclair D, McKenna A, Heinrich MC, Frank DA, Meyerson M.

Nat Genet. 2013 Feb;45(2):131-2. doi: 10.1038/ng.2522. Epub 2013 Jan 13.

PMID:
23313954
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Exome versus transcriptome sequencing in identifying coding region variants.

Ku CS, Wu M, Cooper DN, Naidoo N, Pawitan Y, Pang B, Iacopetta B, Soong R.

Expert Rev Mol Diagn. 2012 Apr;12(3):241-51. doi: 10.1586/erm.12.10. Review.

PMID:
22468815
[PubMed - indexed for MEDLINE]
3.

Exome sequencing as a tool for Mendelian disease gene discovery.

Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J.

Nat Rev Genet. 2011 Sep 27;12(11):745-55. doi: 10.1038/nrg3031. Review.

PMID:
21946919
[PubMed - indexed for MEDLINE]
4.

Somatic and visceral solitary fibrous tumors in the abdomen and pelvis: cross-sectional imaging spectrum.

Shanbhogue AK, Prasad SR, Takahashi N, Vikram R, Zaheer A, Sandrasegaran K.

Radiographics. 2011 Mar-Apr;31(2):393-408. doi: 10.1148/rg.312105080. Review.

PMID:
21415186
[PubMed - indexed for MEDLINE]
5.

Molecular genetic studies of complex phenotypes.

Marian AJ.

Transl Res. 2012 Feb;159(2):64-79. doi: 10.1016/j.trsl.2011.08.001. Epub 2011 Aug 31. Review.

PMID:
22243791
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

SYT-SSX fusion genes in synovial sarcoma of the thorax.

Yano M, Toyooka S, Tsukuda K, Dote H, Morimoto Y, Ohata N, Ichimura K, Aoe M, Date H, Shimizu N.

Lung Cancer. 2004 Jun;44(3):391-7. Review.

PMID:
15140553
[PubMed - indexed for MEDLINE]
7.

Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies.

Chou J, Ohsumi TK, Geha RS.

Curr Opin Allergy Clin Immunol. 2012 Dec;12(6):623-8. doi: 10.1097/ACI.0b013e3283588ca6. Review.

PMID:
23095910
[PubMed - indexed for MEDLINE]
8.

Next-generation sequencing to identify genetic causes of cardiomyopathies.

Norton N, Li D, Hershberger RE.

Curr Opin Cardiol. 2012 May;27(3):214-20. doi: 10.1097/HCO.0b013e328352207e. Review.

PMID:
22421630
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk