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BMC Bioinformatics|May 31, 2008
BatchPrimer3: a high throughput web application for PCR and sequencing primer designFrank M You, Naxin Huo, Yong Qiang Gu, et al.
Archives of Iranian Medicine|February 4, 2016
Mutation in TWINKLE in a Large Iranian Family with Progressive External Ophthalmoplegia, Myopathy, Dysphagia and Dysphonia, and Behavior ChangeAbbas Tafakhori, Alvin Yu Jin Ng, Sumanty Tohari, et al.
Advances in Radiation Oncology|December 22, 2021
Site-Specific Education Using Digital Media to Improve Patient Understanding of the Radiotherapy Trajectory: An Interventional StudyHussain Almerdhemah, Zaheeda Mulla, Hane Mohammad Muamenah, et al.
American Journal of Human Genetics|April 3, 2012
Exome sequencing identifies PDE4D mutations in acrodysostosisHane Lee, John M Graham, David L Rimoin, et al.
Journal of Medical Genetics|July 1, 1997
A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28G S Pai, B Hane, M Joseph, et al.
Revue Des Maladies Respiratoires|February 3, 2007
[Familial tuberculosis: tracing the contacts of an infectious case]A Diatta, N O Toure, Y Dia Kane, et al.
The Journal of Biological Chemistry|March 10, 2015
Rapid Trimming of Cell Surface Polysialic Acid (PolySia) by Exovesicular Sialidase Triggers Release of Preexisting Surface NeurotrophinMizuki Sumida, Masaya Hane, Uichiro Yabe, et al.
Early Human Development|September 13, 2021
Preterm infant heart rate is lowered after Family Nurture Intervention in the NICU: Evidence in support of autonomic conditioningRobert J Ludwig, Ruth E Grunau, Julia E Chafkin, et al.
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