Showing results (111-120 of 121) with videos related to
Sort By:
Pageof 13
Acta Anaesthesiologica Scandinavica|May 8, 2009
Association between central venous pressure and blood loss during hepatic resection in 984 living donorsY K Kim, J H Chin, S J Kang, et al.Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
Microsatellites provide evidence for Y chromosome diversity among the founders of the New WorldA Ruiz-Linares, D Ortíz-Barrientos, M Figueroa, et al.BJOG : an International Journal of Obstetrics and Gynaecology|August 19, 2021
Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?R Mellis, R Y Eberhardt, S J Hamilton, et al.Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.Annals of Human Genetics|April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspectiveC Capelli, N Redhead, V Romano, et al.Epilepsy Research|November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsyJ M Lynch, S K Tate, P Kinirons, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
The alpha-synuclein gene in multiple system atrophyT Ozawa, D G Healy, P M Abou-Sleiman, et al.Journal of Viral Hepatitis|April 14, 2012
Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment responseP J Clark, A J Thompson, M Zhu, et al.Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.American Journal of Human Genetics|June 19, 1998
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypesJ C Stephens, D E Reich, D B Goldstein, et al.Pageof 13