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32199 publications found in the database

*2012 (1980)

*Starting in 2010, coverage has been refocused on core journals.

2012 Publications

Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion
Neira, V. A. et al. American Journal of Medical Genetics Part a 158A(6), 1498-502, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region
Michelson, M. et al. American Journal of Medical Genetics Part a 158A(6), 1395-9, 2012  PubMed

A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1
Fahrner, J. A. et al. American Journal of Medical Genetics Part a 158A(6), 1414-21, 2012, CustomExpress Arrays  PubMed

Transcription factor Olig2 defines subpopulations of retinal progenitor cells biased toward specific cell fates
Hafler, B. P. et al. Proceedings of the National Academy of Sciences of the United States of America 109(20), 7882-7, 2012  PubMed

Common PIK3CA Mutants and a Novel 3' UTR Mutation Are Associated with Increased Sensitivity to Saracatinib
Arcaroli, J. J. et al. Clinical Cancer Research 18(9), 2704-14, 2012, Human Gene 1.0 ST Array  PubMed

Protection from liver fibrosis by a peroxisome proliferator-activated receptor delta agonist
Iwaisako, K. et al. Proceedings of the National Academy of Sciences of the United States of America 109(21), E1369-76, 2012, Mouse Genome 430 2.0 Array  PubMed

A cluster of cooperating tumor-suppressor gene candidates in chromosomal deletions
Xue, W. et al. Proceedings of the National Academy of Sciences of the United States of America 109(21), 8212-7, 2012, Human Genome U133A 2.0 Array  PubMed

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Celestino-Soper, P. B. S. et al. Proceedings of the National Academy of Sciences of the United States of America 109(21), 7974-81, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Genome-wide association study of primary open angle glaucoma risk and quantitative traits
Gibson, J. et al. Molecular Vision 18(115), 1083-92, 2012, Genome-Wide Human SNP Array 6.0  PubMed

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