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Electrophoresis|August 6, 1999
Informativity assessment for biallelic single nucleotide polymorphismsM KrawczakClinical Genetics|February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's diseaseM A Martín, J C Rubio, A García, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Algorithms for the restriction-site mapping of DNA moleculesM KrawczakHuman Genetics|April 1, 1995
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein CP J Hallam, A I Wacey, P M Mannucci, et al.Blood|August 15, 1991
Recurrent deletion in the human antithrombin III geneC B Grundy, F Thomas, D S Millar, et al.Electrophoresis|January 1, 1995
An informativity index for multilocus DNA fingerprintsM Krawczak, T LubjuhnBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1995
Functional analysis of an unusual length polymorphism in the human antithrombin III (AT3) gene promoterP C Winter, D A Scopes, L P Berg, et al.Human Genetics|February 24, 2001
Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergenceH Winter, L Langbein, M Krawczak, et al.Electrophoresis|January 1, 1992
A genetic factor model for the statistical analysis of multilocus DNA fingerprintsM Krawczak, B BockelPageof 26