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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.
Methods in Molecular Biology (Clifton, N.J.)|September 3, 2013
self-assembling GFP: a versatile tool for plant (membrane) protein analysesKatharina Wiesemann, Lucia E Groß, Manuel Sommer, et al.
European Journal of Cardiology|March 1, 1979
Transient left anterior hemiblock during angina pectoris: coronarographic aspects and clinical significanceS Lévy, R Gérard, A Castellanos, et al.
Plos One|December 29, 2010
Three ways of combining genotyping and resequencing in case-control association studiesJeffrey A Longmate, Garrett P Larson, Theodore G Krontiris, 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.
The International Journal of Neuropsychopharmacology|June 26, 2014
The dopamine reuptake inhibitor MRZ-9547 increases progressive ratio responding in ratsS Sommer, W Danysz, H Russ, et al.
Human Mutation|December 26, 2001
Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutationsJinong Feng, Joni B Drost, William A Scaringe, et al.
Molecular Genetics and Metabolism|October 3, 2002
Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathyJinong Feng, Jin Yan, Carolyn H Buzin, et al.
Trends in Biotechnology|January 22, 2005
Proofreading genotyping assays mediated by high fidelity exo+ DNA polymerasesJia Zhang, Kai Li, Jose R Pardinas, et al.
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