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Mayo Clinic Proceedings|May 1, 1987
Application of DNA-based diagnosis to patient care: the example of hemophilia AS S Sommer, J L SobellBiotechniques|May 25, 1999
Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivityQ Liu, J Feng, C Buzin, et al.Human Genetics|August 1, 1991
Identification of mutations in two families with sporadic hemophilia AC Paynton, G Sarkar, S S SommerNucleic Acids Research|February 11, 1991
Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogenyG Sarkar, C Paynton, S S SommerChinese Medical Journal|October 12, 2001
PCR assay for the inversion causing severe Hemophilia A and its applicationJ Liu, Q Liu, Y Liang, et al.American Journal of Human Genetics|August 1, 1993
Characterization of the patterns of polymorphism in a "cryptic repeat" reveals a novel type of hypervariable sequenceD P Jacobson, P Schmeling, S S SommerMutation Research|November 11, 1996
Towards validation of the Big Blue transgenic mouse mutagenesis assay: the mutational spectrum of ex vivo pinpoint mutant plaquesH Nishino, V L Buettner, S S SommerGenomics|January 1, 1990
Direct sequencing of the activation peptide and the catalytic domain of the factor IX gene in six speciesG Sarkar, D D Koeberl, S S SommerAmerican Journal of Human Genetics|January 1, 1992
From molecular variant to disease: initial steps in evaluating the association of transthyretin M119 with diseaseS Ii, J L Sobell, S S SommerAmerican Journal of Human Genetics|May 1, 1994
The rates of G:C-->T:A and G:C-->C:G transversions at CpG dinucleotides in the human factor IX geneR P Ketterling, E Vielhaber, S S SommerPageof 388