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Arteriosclerosis, Thrombosis, and Vascular Biology|July 5, 2003
Human CRP gene polymorphism influences CRP levels: implications for the prediction and pathogenesis of coronary heart diseaseD J Brull, Norma Serrano, F Zito, et al.
Nucleic Acids Research|September 12, 1988
Truncated variants of apolipoprotein B cause hypobetalipoproteinaemiaD R Collins, T J Knott, R J Pease, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2012
Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situA P Walker, R C Fowkes, F Saleh, et al.
Journal of Medical Genetics|July 25, 1998
Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of ScotlandW K Lee, L Haddad, M J Macleod, et al.
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