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Fiona Watkins

Showing results (1-10 of 7) with videos related to

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American Journal of Hematology|July 30, 2004
Mutations in PTPN11 are rare in adult myelodysplastic syndromes and acute myeloid leukemiaFiona Watkins, Carrie Fidler, Jacqueline Boultwood, et al.
Haematologica|July 20, 2004
NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q)Carrie Fidler, Fiona Watkins, David T Bowen, et al.
British Journal of Haematology|August 4, 2004
Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemiaJacqueline Boultwood, Andrea Pellagatti, Fiona Watkins, et al.
Blood|May 31, 2002
Narrowing and genomic annotation of the commonly deleted region of the 5q- syndromeJacqueline Boultwood, Carrie Fidler, Amanda J Strickson, et al.
Blood|June 28, 2003
Phenotype and genotype of interfollicular large B cells, a subpopulation of lymphocytes often with dendritic morphologyTeresa Marafioti, Margaret Jones, Fabio Facchetti, et al.
European Journal of Human Genetics : EJHG|April 7, 2026
Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomaliesFabiola Ceroni, Linda M Reis, Fiona Watkins, et al.
British Journal of Haematology|May 19, 2004
Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technologyAndrea Pellagatti, Noor Esoof, Fiona Watkins, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Hematology|July 30, 2004
Mutations in PTPN11 are rare in adult myelodysplastic syndromes and acute myeloid leukemiaFiona Watkins, Carrie Fidler, Jacqueline Boultwood, et al.
Haematologica|July 20, 2004
NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q)Carrie Fidler, Fiona Watkins, David T Bowen, et al.
British Journal of Haematology|August 4, 2004
Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemiaJacqueline Boultwood, Andrea Pellagatti, Fiona Watkins, et al.
Blood|May 31, 2002
Narrowing and genomic annotation of the commonly deleted region of the 5q- syndromeJacqueline Boultwood, Carrie Fidler, Amanda J Strickson, et al.
Blood|June 28, 2003
Phenotype and genotype of interfollicular large B cells, a subpopulation of lymphocytes often with dendritic morphologyTeresa Marafioti, Margaret Jones, Fabio Facchetti, et al.
European Journal of Human Genetics : EJHG|April 7, 2026
Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomaliesFabiola Ceroni, Linda M Reis, Fiona Watkins, et al.
British Journal of Haematology|May 19, 2004
Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technologyAndrea Pellagatti, Noor Esoof, Fiona Watkins, et al.
Pageof 1