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D M Layton

Showing results (11-20 of 51) with videos related to

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Lancet (London, England)|November 7, 1987
Treatment for myelodysplastic syndromesA Pagliuca, D M Layton, G J Mufti
Blood Reviews|September 1, 1995
Hereditary red cell enzymopathiesR Arya, D M Layton, A J Bellingham
Blood Cells, Molecules & Diseases|November 27, 1999
The consequence of nucleotide substitutions in the triosephosphate isomerase (TPI) gene promoterA Humphries, A Ationu, B Wild, et al.
Blood Cells, Molecules & Diseases|November 27, 1999
Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopeniaL J Thompson, M R Lalloz, D M Layton
BMJ (Clinical Research Ed.)|December 3, 1988
Hyperinfection with strongyloides after treatment for adult T cell leukaemia-lymphoma in an African immigrantA Pagliuca, D M Layton, S Allen, et al.
Human Genetics|August 24, 1999
Ancestral origin of variation in the triosephosphate isomerase gene promoterA Humphries, A Ationu, M R Lalloz, et al.
Blood Cells, Molecules & Diseases|January 11, 2002
Nucleotide variation regulates the level of enhancement by hypersensitive site 2 of the beta-globin locus control regionS F Ofori-Acquah, M R Lalloz, D M Layton
Biochemical and Biophysical Research Communications|January 28, 1999
Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomesS F Ofori-Acquah, M R Lalloz, D M Layton
Human Mutation|January 1, 1997
Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiencyR Arya, M R Lalloz, A J Bellingham, et al.
Leukemia|March 1, 1991
Cross-lineage rearrangement of antigen receptor genes in atypical chronic myeloid leukemiaM H Mangi, D M Layton, K Tobal, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Lancet (London, England)|November 7, 1987
Treatment for myelodysplastic syndromesA Pagliuca, D M Layton, G J Mufti
Blood Reviews|September 1, 1995
Hereditary red cell enzymopathiesR Arya, D M Layton, A J Bellingham
Blood Cells, Molecules & Diseases|November 27, 1999
The consequence of nucleotide substitutions in the triosephosphate isomerase (TPI) gene promoterA Humphries, A Ationu, B Wild, et al.
Blood Cells, Molecules & Diseases|November 27, 1999
Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopeniaL J Thompson, M R Lalloz, D M Layton
BMJ (Clinical Research Ed.)|December 3, 1988
Hyperinfection with strongyloides after treatment for adult T cell leukaemia-lymphoma in an African immigrantA Pagliuca, D M Layton, S Allen, et al.
Human Genetics|August 24, 1999
Ancestral origin of variation in the triosephosphate isomerase gene promoterA Humphries, A Ationu, M R Lalloz, et al.
Blood Cells, Molecules & Diseases|January 11, 2002
Nucleotide variation regulates the level of enhancement by hypersensitive site 2 of the beta-globin locus control regionS F Ofori-Acquah, M R Lalloz, D M Layton
Biochemical and Biophysical Research Communications|January 28, 1999
Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomesS F Ofori-Acquah, M R Lalloz, D M Layton
Human Mutation|January 1, 1997
Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiencyR Arya, M R Lalloz, A J Bellingham, et al.
Leukemia|March 1, 1991
Cross-lineage rearrangement of antigen receptor genes in atypical chronic myeloid leukemiaM H Mangi, D M Layton, K Tobal, et al.
Pageof 6