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32199 publications found in the database

*2010 (1822)

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

2010 Publications

Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami
Huyghe, J. R. et al. European Journal of Human Genetics 18(5), 569-74, 2010, Mapping 100K Set  PubMed

A Maternally Inherited Chromosome 18q22.1 Deletion in a Male With Late-Presenting Diaphragmatic Hernia and Microphthalmia-Evaluation of DSEL as a Candidate Gene for the Diaphragmatic Defect
Zayed, H. et al. American Journal of Medical Genetics Part a 152A(4), 916-23, 2010, Mapping 100K Set  PubMed

Mutations in FLVCR1 Cause Posterior Column Ataxia and Retinitis Pigmentosa
Raiadhyaksha, A. M. et al. American Journal of Human Genetics 87(5), 643-54, 2010, Mapping 100K Set  PubMed

European admixture on the Micronesian island of Kosrae: lessons from complete genetic information
Bonnen, P. E. et al. European Journal of Human Genetics 18(3), 309-16, 2010, Mapping 100K Set  PubMed

Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome
Schneppenheim, R. et al. American Journal of Human Genetics 86(2), 279-84, 2010, Mapping 100K Set  PubMed

Identification of DOK genes as lung tumor suppressors
Berger, A. H. et al. Nature Genetics 42(3), NPG, 2010, Mapping 100K Set  PubMed

Biallelic mutation of Protocadherin-21 (PCDH21) causes retinal degeneration in humans
Henderson, R. H. et al. Molecular Vision 16(6-7), 46-52, 2010, Mapping 100K Set  PubMed

The promyelocytic leukemia zinc-finger gene, PLZF, is frequently downregulated in malignant mesothelioma cells and contributes to cell survival
Cheung, M. et al. Oncogene 29(11), 1633-40, 2010, Mapping 100K Set  PubMed

New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: Detection of candidate regions by homozygosity mapping
Pereiro, I. et al. Molecular Vision 16(17), 137-43, 2010, Mapping 100K Set  PubMed

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