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Clinical Genetics|September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Journal of the American Chemical Society|May 10, 2012
Rendering protein-based particles transiently insoluble for therapeutic applicationsJing Xu, Jin Wang, J Christopher Luft, et al.
Journal of Natural Products|April 20, 2018
Absolute Configuration and Pharmacology of the Poison Frog Alkaloid PhantasmidineRichard W Fitch, Barry B Snider, Quan Zhou, et al.
Chemical Biology & Drug Design|September 12, 2015
Targeting Bacterial Cell Wall Peptidoglycan Synthesis by Inhibition of Glycosyltransferase ActivityMichael F Mesleh, Premraj Rajaratnam, Mary Conrad, et al.
American Journal of Human Genetics|August 27, 1998
Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distributionP Malaspina, F Cruciani, B M Ciminelli, et al.
Human Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 3, 2009
A global survey of the role of ultraviolet radiation and hormonal influences in the development of melasmaJ P Ortonne, I Arellano, M Berneburg, et al.
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