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32199 publications found in the database

*2013 (2117)

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

2013 Publications

Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood
Mehta, D. et al. European Journal of Human Genetics 21(1), 48-54, 2013  PubMed

Limited Gene Expression Variation in Human Embryonic Stem Cell and Induced Pluripotent Stem Cell-Derived Endothelial Cells
White, M. P. et al. Stem Cells 31(1), 92-103, 2013, Human Gene 1.0 ST Array  PubMed

A Case of Cerebral Hypomyelination With Spondylo-epi-Metaphyseal Dysplasia
Kimura-Ohba, S. et al. American Journal of Medical Genetics Part a 161A(1), 203-7, 2013  PubMed

The Effect of Genomic Inversions on Estimation of Population Genetic Parameters from SNP Data
al Basatena, N. K. S. et al. Genetics 193(1), 243-53, 2013  PubMed

Maternal Transmission of Interstitial 8p23.1 Deletion Detected During Prenatal Diagnosis
Guimiot, F. et al. American Journal of Medical Genetics Part a 161A(1), 208-13, 2013  PubMed

Haplotype-based profiling of subtle allelic imbalance with SNP arrays
Vattathil, S. et al. Genome Research 23(1), 152-8, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Clinical Utility of the X-Chromosome Array
Zarate, Y. A. et al. American Journal of Medical Genetics Part a 161A(1), 120-30, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Duplication of 20p12.3 Associated With Familial Wolff-Parkinson-White Syndrome
Mills, K. I. et al. American Journal of Medical Genetics Part a 161A(1), 137-44, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Severe Craniosynostosis in an Infant With Deletion 22q11.2 Syndrome
Al-Hertani, W. et al. American Journal of Medical Genetics Part a 161A(1), 153-7, 2013, Genome-Wide Human SNP Array 6.0  PubMed

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