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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.Obstetrics and Gynecology|September 1, 1989
Accurate prenatal diagnosis with novel polymerase chain reaction primers in a family with sporadic hemophilia AG Sarkar, M I Evans, S Kogan, 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.Mutation Research|October 12, 2000
Evidence that proximal multiple mutations in Big Blue transgenic mice are dependent eventsV L Buettner, K A Hill, W A Scaringe, et al.Human Genetics|May 1, 1992
Missense mutations and the magnitude of functional deficit: the example of factor IXS S Sommer, E J Bowie, R P Ketterling, et al.American Journal of Medical Genetics|July 15, 1993
Dopamine D4 receptor variants in unrelated schizophrenic cases and controlsS S Sommer, T J Lind, L L Heston, et al.Genomics|August 1, 1991
Evidence that descendants of three founders constitute about 25% of hemophilia B in the United StatesR P Ketterling, C D Bottema, J A Phillips, et al.Mayo Clinic Proceedings|November 1, 1989
A novel method for detecting point mutations or polymorphisms and its application to population screening for carriers of phenylketonuriaS S Sommer, J D Cassady, J L Sobell, et al.Mutation Research|January 8, 1999
Spontaneous mutations in the Big Blue transgenic system are primarily mouse derivedK A Hill, V L Buettner, B W Glickman, et al.Pageof 389