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32199 publications found in the database

*2010 (1822)

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

2010 Publications

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot
Rauch, R. et al. Journal of Medical Genetics 47(5), 321-31, 2010, Mapping 100K Set  PubMed

L-Histidine Decarboxylase and Tourette's Syndrome
Ercan-Sencicek, A. G. et al. New England Journal of Medicine 362(20), 1901-8, 2010, Mapping 100K Set  PubMed

A genome-wide association study for age-related hearing impairment in the Saami
Van Laer, L. et al. European Journal of Human Genetics 18(6), 685-93, 2010, Mapping 100K Set  PubMed

Discovery and Functional Analysis of a Retinitis Pig mentosa Gene, C2ORF71
Nishimura, D. Y. et al. American Journal of Human Genetics 86(5), 686-95, 2010, Mapping 100K Set  PubMed

A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy
Mukhopadhyay, R. et al. Molecular Vision 16(61), 540-8, 2010, Mapping 100K Set  PubMed

Mandibulofacial Dysostosis, Severe Lower Eyelid Coloboma, Cleft Palate, and Alopecia: A New Distinct Form of Mandibulofacial Dysostosis or a Severe Form of Johnson-McMillin Syndrome?
Zechi-Ceide, R. M. et al. American Journal of Medical Genetics Part a 152A(7), 1838-40, 2010, Mapping 100K Set  PubMed

Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect
Antonicka, H. et al. American Journal of Human Genetics 87(1), 115-22, 2010, Mapping 100K Set  PubMed

Gene Flow between the Korean Peninsula and Its Neighboring Countries
Jung, J. et al. Plos One 5(7), NPG, 2010, Mapping 100K Set  PubMed

Trisomy 16q21 --> qter: Seven-Year Follow-Up of a Girl With Unusually Long Survival
de Carvalho, A. F. L. et al. American Journal of Medical Genetics Part a 152A(8), 2074-8, 2010, Mapping 100K Set  PubMed

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