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32199 publications found in the database

*2010 (1822)

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

2010 Publications

Infantile Cerebral and Cerebellar Atrophy Is Associated with a Mutation in the MED17 Subunit of the Transcription Preinitiation Mediator Complex
Kaufmann, R. et al. American Journal of Human Genetics 87(5), 667-70, 2010, Human Mapping 500K Array SetMapping 500K  PubMed

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
Hamdan, F. F. et al. American Journal of Human Genetics 87(5), 671-8, 2010  PubMed

Patterns and Processes of Genome-Wide Divergence Between North American and African Drosophila melanogaster
Yukilevich, R. et al. Genetics 186(1), NPG, 2010, Drosophila Tiling 1.0R Array  PubMed

Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB
Scheuermann, J. C. et al. Nature 465(7295), NPG, 2010, Drosophila Tiling 1.0R Array  PubMed

MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes
Sirmacid, A. et al. American Journal of Human Genetics 87(5), 679-86, 2010, Genome-Wide Human SNP Array 6.0  PubMed

Adverse interactions between micro-RNAs and target genes from different species
Tang, T. et al. Proceedings of the National Academy of Sciences of the United States of America 107(29), 12935-40, 2010, Drosophila Tiling 1.0R Array  PubMed

Aire's Partners in the Molecular Control of Immunological Tolerance
Abramson, J. et al. Cell 140(1), 123-35, 2010  PubMed

A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13 1 Microdeletion Syndromes
Shhen, A. et al. American Journal of Human Genetics 87(5), 631-42, 2010  PubMed

Paternal Uniparental Isodisomy of Chromosome 6 Causing a Complex Syndrome Including Complete IFN-gamma Receptor 1 Deficiency
Prando, C. et al. American Journal of Medical Genetics Part a 152A(3), 622-9, 2010, Genome-Wide Human SNP Array 6.0  PubMed

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