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32199 publications found in the database

*2015 (1336)

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

2015 Publications

Comparative Genomic, MicroRNA, and Tissue Analyses Reveal Subtle Differences between Non-Diabetic and Diabetic Foot Skin
Ramirez, H. A. et al. Plos One 10(8), NPG, 2015, Human Gene 2.0 ST Array  PubMed

Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility
Wang, J. C. et al. European Journal of Human Genetics 23(5), 663-71, 2015  PubMed

Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia
Kaiser, A. S. et al. European Journal of Human Genetics 23(5), 704-7, 2015, CytoScan  PubMed

An Infant with Large Fontanelles, Aplasia Cutis Congenita, Tessier Facial Cleft, Polydactyly Inversus, and Toe Syndactyly: A Previously Undescribed Syndrome?
Jackson, J. et al. American Journal of Medical Genetics Part a 167A(4), 683-7, 2015, CytoScan  PubMed

Digital PCR Validates 8q Dosage as Prognostic Tool in Uveal Melanoma
Versluis, M. et al. Plos One 10(3), NPG, 2015  PubMed

Persistence of Mullerian Duct Structures in a Genetic Male With Distal Monosomy 10q
Tosur, M. et al. American Journal of Medical Genetics Part a 167A(4), 791-6, 2015, CytoScan  PubMed

Mosaic Trisomy 15 in a Liveborn Infant
McPadden, J. et al. American Journal of Medical Genetics Part a 167A(4), 821-5, 2015, CytoScan  PubMed

Identification of ncRNAs as potential therapeutic targets in multiple sclerosis through differential ncRNA - mRNA network analysis
Irizar, H. et al. BMC Genomics 16(), NPG, 2015  PubMed

Diagnosis of 9q22.3 Microdeletion Syndrome In Utero Following Identification of Craniosynostosis, Overgrowth, and Skeletal Anomalies
Reichert, S. C. et al. American Journal of Medical Genetics Part a 167A(4), 862-5, 2015, CytoScan  PubMed

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