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T Vulliamy

Showing results (11-20 of 32) with videos related to

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British Journal of Haematology|September 1, 1995
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD geneA Rovira, T Vulliamy, M A Pujades, et al.
American Journal of Human Genetics|November 1, 1993
Exon skipping and translation in patients with frameshift deletions in the dystrophin geneT G Sherratt, T Vulliamy, V Dubowitz, et al.
British Journal of Haematology|February 13, 2001
Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformationM McCloy, A Almeida, P Daly, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC diseaseK Konstantopoulos, T Vulliamy, D Swirsky, et al.
European Journal of Haematology|July 1, 1991
Non-lymphoid blast crisis of CML with rearrangement of immunoglobulin and T-cell receptor delta genesA Bashey, T Vulliamy, B S Cai, et al.
British Journal of Haematology|October 1, 1994
Management of pregnancy when maternal blood has a very high level of fetal haemoglobinJ S Kaeda, K Prasad, R J Howard, et al.
Human Mutation|January 1, 1996
Independent origin of single and double mutations in the human glucose 6-phosphate dehydrogenase geneT Vulliamy, A Rovira, N Yusoff, et al.
Clinical Genetics|January 5, 2011
Telomere length measurement can distinguish pathogenic from non-pathogenic variants in the shelterin component, TIN2T Vulliamy, R Beswick, M J Kirwan, et al.
Nature|September 28, 2001
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenitaT Vulliamy, A Marrone, F Goldman, et al.
Journal of Medical Genetics|December 1, 1996
Fine mapping of the dyskeratosis congenita locus in Xq28S W Knight, T Vulliamy, G L Forni, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|September 1, 1995
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD geneA Rovira, T Vulliamy, M A Pujades, et al.
American Journal of Human Genetics|November 1, 1993
Exon skipping and translation in patients with frameshift deletions in the dystrophin geneT G Sherratt, T Vulliamy, V Dubowitz, et al.
British Journal of Haematology|February 13, 2001
Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformationM McCloy, A Almeida, P Daly, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC diseaseK Konstantopoulos, T Vulliamy, D Swirsky, et al.
European Journal of Haematology|July 1, 1991
Non-lymphoid blast crisis of CML with rearrangement of immunoglobulin and T-cell receptor delta genesA Bashey, T Vulliamy, B S Cai, et al.
British Journal of Haematology|October 1, 1994
Management of pregnancy when maternal blood has a very high level of fetal haemoglobinJ S Kaeda, K Prasad, R J Howard, et al.
Human Mutation|January 1, 1996
Independent origin of single and double mutations in the human glucose 6-phosphate dehydrogenase geneT Vulliamy, A Rovira, N Yusoff, et al.
Clinical Genetics|January 5, 2011
Telomere length measurement can distinguish pathogenic from non-pathogenic variants in the shelterin component, TIN2T Vulliamy, R Beswick, M J Kirwan, et al.
Nature|September 28, 2001
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenitaT Vulliamy, A Marrone, F Goldman, et al.
Journal of Medical Genetics|December 1, 1996
Fine mapping of the dyskeratosis congenita locus in Xq28S W Knight, T Vulliamy, G L Forni, et al.
Pageof 4