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32199 publications found in the database

*2014 (1694)

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

2014 Publications

AtRH57, a DEAD-box RNA helicase, is involved in feedback inhibition of glucose- mediated abscisic acid accumulation during seedling development and additively affects pre- ribosomal RNA processing with high glucose
Hsu, Y. F. et al. Plant Journal 77(1), 119-35, 2014, Arabidopsis ATH1 Genome Array  PubMed

Characterization of Core Clinical Phenotypes Associated With Recurrent Proximal 15q25.2 Microdeletions
Burgess, T. et al. American Journal of Medical Genetics Part a 164(1), 77-86, 2014  PubMed

A Meta-Analysis of MicroRNA Expression in Liver Cancer
Yang, J. C. et al. Plos One 9(12), NPG, 2014, miRNA Array  PubMed

A Clinical Study of Patients With Pericentromeric Deletion and Duplication Within 16p12.2-p11.2
Okamoto, N. et al. American Journal of Medical Genetics Part a 164(1), 213-9, 2014  PubMed

Aortic Aneurysm and Craniosynostosis in a Family With Cantu Syndrome
Hiraki, Y. et al. American Journal of Medical Genetics Part a 164(1), 231-6, 2014  PubMed

X Chromosome Exome Sequencing Reveals a Novel ALG13 Mutation in a Nonsyndromic Intellectual Disability Family With Multiple Affected Male Siblings
Bissar-Tadmouri, N. et al. American Journal of Medical Genetics Part a 164(1), 164-9, 2014, Genome-Wide Human SNP Array 6.0  PubMed

Frequency of Prenatal Cytogenetic Diagnosis and Pregnancy Outcomes by Maternal Race- Ethnicity, and the Effect on the Prevalence of Trisomy 21, Metropolitan Atlanta, 1996-2005
Jackson, J. M. et al. American Journal of Medical Genetics Part a 164(1), 70-6,77-87, 2014  PubMed

Giant Breast Tumors in a Patient With Beckwith-Wiedemann Syndrome
Cappuccio, G. et al. American Journal of Medical Genetics Part a 164(1), 182-5, 2014  PubMed

Hemiconvulsion-Hemiplegia-Epilepsy Syndrome With 1q44 Microdeletion: Causal or Chance Association 1
Gupta, R. et al. American Journal of Medical Genetics Part a 164(1), 186-9, 2014  PubMed

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