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American Journal of Medical Genetics|May 19, 2000
Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophyK Saito, M Osawa, Z P Wang, et al.
Physical Review Letters|April 1, 2014
Electronic excitations of a magnetic impurity state in the diluted magnetic semiconductor (Ga,Mn)AsM Kobayashi, H Niwa, Y Takeda, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndromeT Kosho, K Muroya, T Nagai, et al.
Journal of Synchrotron Radiation|May 12, 2006
Standard transport channels of X-ray beamlines at SPring-8S Goto, M Yabashi, H Ohashi, et al.
Nature Genetics|October 1, 1996
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndromeI Hatada, H Ohashi, Y Fukushima, et al.
Physical Review Letters|June 4, 2008
Revisiting the valence-band and core-level photoemission spectra of NiOM Taguchi, M Matsunami, Y Ishida, et al.
Nephron|September 16, 1998
Plasma soluble fas and soluble fas ligand in chronic glomerulonephritisH Sano, K Asano, S Minatoguchi, et al.
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