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A P Walker

Showing results (121-130 of 127) with videos related to

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Prenatal Diagnosis|January 1, 1991
Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphismsN G Laing, A P Walker, P A Akkari, et al.
Nucleic Acids Research|April 11, 1990
D21S194, a jump clone from D21S16A P Walker, F S Collins, T Siddique, et al.
American Journal of Human Genetics|June 1, 1991
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkageM A Pericak-Vance, J L Bebout, P C Gaskell, et al.
Clinical Genetics|February 3, 2006
Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening StudyJ C Barton, R T Acton, L Lovato, et al.
Environmental Science & Technology|January 30, 2009
Effect of fuel and lube oil sulfur on the performance of a diesel exhaust gas continuously regenerating trapD B Kittelson, W F Watts, J P Johnson, et al.
Nature Genetics|November 5, 1999
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis ConsortiumA T Merryweather-Clarke, J J Pointon, J D Shearman, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 27, 2010
A summary report of the COLIPA international validation study on alternatives to the draize rabbit eye irritation testP G Brantom, L H Bruner, M Chamberlain, et al.
Pageof 13

Showing results (121-130 of 127) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 127 results.
Prenatal Diagnosis|January 1, 1991
Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphismsN G Laing, A P Walker, P A Akkari, et al.
Nucleic Acids Research|April 11, 1990
D21S194, a jump clone from D21S16A P Walker, F S Collins, T Siddique, et al.
American Journal of Human Genetics|June 1, 1991
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkageM A Pericak-Vance, J L Bebout, P C Gaskell, et al.
Clinical Genetics|February 3, 2006
Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening StudyJ C Barton, R T Acton, L Lovato, et al.
Environmental Science & Technology|January 30, 2009
Effect of fuel and lube oil sulfur on the performance of a diesel exhaust gas continuously regenerating trapD B Kittelson, W F Watts, J P Johnson, et al.
Nature Genetics|November 5, 1999
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis ConsortiumA T Merryweather-Clarke, J J Pointon, J D Shearman, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 27, 2010
A summary report of the COLIPA international validation study on alternatives to the draize rabbit eye irritation testP G Brantom, L H Bruner, M Chamberlain, et al.
Pageof 13