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Human Genetics|December 29, 2000
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regionsM Krawczak, N A Chuzhanova, P D Stenson, et al.Human Mutation|December 29, 1999
Human gene mutation database-a biomedical information and research resourceM Krawczak, E V Ball, I Fenton, et al.Human Genetics|August 1, 1992
Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcriptsR Slomski, M Schloesser, L P Berg, et al.Human Genetics|January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicismK Wieland, D S Millar, C B Grundy, et al.Blood|September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasmaP Simioni, M Kalafatis, D S Millar, et al.Human Genetics|January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IXB Zoll, J Arnemann, M Krawczak, et al.Child Development|August 13, 2015
Knowing When to Be "Rational": Flexible Economic Decision Making and Executive Function in Preschool ChildrenWendy S C Lee, Stephanie M CarlsonJournal of Applied Physiology (Bethesda, Md. : 1985)|June 1, 1996
Catchlike property of human muscle during isovelocity movementsS A Binder-Macleod, S C LeePflugers Archiv : European Journal of Physiology|July 1, 1988
Forskolin effects on the voltage-gated K+ conductance of human T cellsD Krause, S C Lee, C DeutschJournal of Applied Physiology (Bethesda, Md. : 1985)|June 14, 2000
Effects of activation frequency on dynamic performance of human fresh and fatigued musclesS C Lee, S A Binder-MacleodPageof 146