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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 1, 2010
Bone and bone marrow pro-osteoclastogenic cytokines are up-regulated in osteoporosis fragility fracturesP D'Amelio, I Roato, L D'Amico, et al.Human Molecular Genetics|September 25, 1997
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19pC Jodice, E Mantuano, L Veneziano, et al.Brain & Development|October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrumA Iodice, M Carecchio, G Zorzi, et al.Annals of Human Genetics|September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansionsM Frontali, G Sabbadini, A Novelletto, et al.American Journal of Human Genetics|February 17, 2001
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2S Guida, F Trettel, S Pagnutti, et al.Annals of Human Genetics|October 11, 2001
A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean areaP Malaspina, M Tsopanomichalou, T Duman, et al.Pageof 3