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32199 publications found in the database

*2015 (1336)

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

2015 Publications

Genome-wide inbreeding estimation within Lebanese communities using SNP arrays
Jalkh, N. et al. European Journal of Human Genetics 23(10), 1364-9, 2015  PubMed

SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia
Stark, Z. et al. American Journal of Medical Genetics Part a 167(10), 2319-26, 2015, CytoScan  PubMed

De novo 11q13.4q14.3 tetrasomy with uniparental isodisomy for 11q14.3qter
Xiao, B. et al. American Journal of Medical Genetics Part a 167(10), 2327-33, 2015, CytoScan  PubMed

REG(4) is a transcriptional target of GATA6 and is essential for colorectal tumorigenesis
Kawasaki, Y. et al. Scientific Reports 5(), NPG, 2015, Human Gene 2.0 ST Array  PubMed

Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies
Kehrer, M. et al. American Journal of Medical Genetics Part a 167(10), 2406-10, 2015, CytoScan  PubMed

Mosaic paternal genome-wide uniparental isodisomy with down syndrome
Darcy, D. et al. American Journal of Medical Genetics Part a 167(10), 2463-9, 2015, CytoScan  PubMed

The Genus Cerion (Gastropoda: Cerionidae) in the Florida Keys
Shrestha, Y. et al. Plos One 10(9), NPG, 2015, ExoSAP-IT  PubMed

c-MYC is a radiosensitive locus in human breast cells
Wade, M. A. et al. Oncogene 34(38), 4985-94, 2015  PubMed

Multi-platform assessment of transcriptional profiling technologies utilizing a precise probe mapping methodology
Yu, J. S. et al. BMC Genomics 16(), NPG, 2015  PubMed

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