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American Journal of Medical Genetics|April 24, 1995
Screening the dopamine D1 receptor gene in 131 schizophrenics and eight alcoholics: identification of polymorphisms but lack of functionally significant sequence changesQ Liu, J L Sobell, L L Heston, et al.Environmental and Molecular Mutagenesis|June 26, 2001
Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificityA Halangoda, J G Still, K A Hill, et al.Journal of Thrombosis and Haemostasis : JTH|January 27, 2005
The incidence of venous thromboembolism among Factor V Leiden carriers: a community-based cohort studyJ A Heit, J L Sobell, H Li, et al.The Journal of Biological Chemistry|November 5, 1985
Photoaffinity labeling of the cap-binding protein complex with ATP/dATP. Differential labeling of free eukaryotic initiation factor 4A and the eukaryotic initiation factor 4A component of the cap-binding protein complex with [alpha-32P]ATP/dATPG Sarkar, I Edery, N SonenbergHuman Mutation|October 3, 2000
Factor IX mutations in South Africans and African Americans are compatible with primarily endogenous influences upon recent germline mutationsX Li, J B Drost, S Roberts, et al.Human Mutation|January 1, 1993
Deletions with inversions: report of a mutation and review of the literatureR P Ketterling, D O Ricke, M W Wurster, et al.American Journal of Human Genetics|September 1, 1989
Functionally important regions of the factor IX gene have a low rate of polymorphism and a high rate of mutation in the dinucleotide CpGD D Koeberl, C D Bottema, J M Buerstedde, et al.Neurology|June 1, 1991
Two-tiered DNA-based diagnosis of transthyretin amyloidosis reveals two novel point mutationsS Ii, S Minnerath, K Ii, et al.American Journal of Medical Genetics|September 20, 1996
Identification of a missense mutation and several polymorphisms in the proenkephalin A gene of schizophrenic patientsM J Mikesell, J L Sobell, S S Sommer, et al.American Journal of Human Genetics|November 1, 1990
The pattern of factor IX germ-line mutation in Asians is similar to that of CaucasiansC D Bottema, R P Ketterling, H S Yoon, et al.Pageof 21