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Annals of Clinical and Laboratory Science|February 29, 2012
A Gly1609Arg missense mutation in the vWF gene in a Korean patient with von Willebrand disease type 2ASeung Jun Choi, Eun-Young Lee, Hee-Jin Kim, et al.
The American Journal of Tropical Medicine and Hygiene|December 7, 2011
Development and evaluation of a rapid diagnostic test for Plasmodium falciparum, P. vivax, and mixed-species malaria antigensGyu-Cheol Lee, Eun-Sung Jeon, Dung Tien Le, et al.
BMC Medical Genetics|May 23, 2008
A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndromeJong-Ha Yoo, Jee-Hyoung Yoo, Yoon-Jung Choi, et al.
Journal of Clinical Laboratory Analysis|September 24, 2009
Oxidative status in iron-deficiency anemiaJong-Ha Yoo, Ho-Young Maeng, Young-Kyu Sun, et al.
Cancer Genetics and Cytogenetics|January 27, 2009
JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literatureJong-Ha Yoo, Tae Sung Park, Ho-Young Maeng, et al.
Haematologica|October 14, 2011
Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP arrayHee-Jin Kim, Duk-Kyung Kim, Ki-Young Yoo, et al.
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