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Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis. J Am Soc Nephrol 2014;25(8):1869-82.
. Consanguinity and hereditary hearing loss in Qatar. Hum Hered 2014;77(1-4):175-82.
. Consanguinity and hereditary hearing loss in Qatar. Hum Hered 2014;77(1-4):175-82.
. Diagnostic accuracy of ultrasonography for hand bony fractures in paediatric patients. Arch Dis Child 2014;99(12):1087-90.
. Differences in time course activation of dorsolateral prefrontal cortex associated with low or high risk choices in a gambling task. Front Hum Neurosci 2014;8:464.
. Expression and replication studies to identify new candidate genes involved in normal hearing function. PLoS One 2014;9(1):e85352.
. F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls. Clin Exp Rheumatol 2014;32(6):993-4.
. Fate of lymphocytes after withdrawal of tofacitinib treatment. PLoS One 2014;9(1):e85463.
. A general approach for haplotype phasing across the full spectrum of relatedness. PLoS Genet 2014;10(4):e1004234.
. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat Genet 2014;46(8):826-36.
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