Showing results (271-280 of 287) with videos related to
Sort By:
Pageof 29
Bioconjugate Chemistry|March 20, 2003
Site-specific PEGylation of hemoglobin at Cys-93(beta): correlation between the colligative properties of the PEGylated protein and the length of the conjugated PEG chainB N Manjula, A Tsai, R Upadhya, et al.Fertility and Sterility|April 20, 2007
Workshop report: evaluation of genetic and epigenetic risks associated with assisted reproductive technologies and infertilityRosanna Weksberg, Cheryl Shuman, Louise Wilkins-Haug, et al.Genetic Epidemiology|October 18, 2002
Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2)Y Zhao, R A Kumar, M E Baser, et al.Arthritis and Rheumatism|February 1, 1985
Immunogenetic studies of juvenile dermatomyositis. III. Study of antibody to organ-specific and nuclear antigensL M Pachman, J M Friedman, M L Maryjowski-Sweeney, et al.Human Heredity|November 30, 2000
Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of MicronesiaD Shmulewitz, S B Auerbach, T Lehner, et al.Tissue Antigens|January 1, 1983
Immunogenetic studies of juvenile dermatomyositis. HLA antigens in patients and their familiesJ M Friedman, L M Pachman, M L Maryjowski, et al.Clinical Genetics|October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotypeI Filges, E Nosova, E Bruder, et al.Neurology|June 16, 2005
Diagnostic criteria for schwannomatosisM MacCollin, E A Chiocca, D G Evans, et al.American Journal of Medical Genetics. Part A|November 12, 2005
Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGHC Tyson, C Harvard, R Locker, et al.American Journal of Medical Genetics|November 15, 2000
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1A E Lin, P H Birch, B R Korf, et al.Pageof 29