David Stevens

发表

haploinsufficiency congenita and aplastic anemia reduce telomerase activity via Heterozygous telomerase RNA mutations found in dyskeratosis

T. Vulliamy, P. Mason, I. Dokal, 2013 .

Heterozygous telomerase RNA mutations found in dyskeratosis congenita and aplastic anemia reduce telomerase activity via haploinsufficiency.

T. Vulliamy, P. Mason, I. Dokal, 2004, Blood.

Absence of mutations in the HoxA10, HoxA11 and HoxD11 nucleotide coding sequences in thrombocytopenia with absent radius syndrome

W. Vainchenker, N. Debili, R. Letestu, 2002, British Journal of Haematology.

Duplex quantitative PCR for molecular monitoring of BCR‐ABL1‐associated hematological malignancies

D. Marin, J. Goldman, L. Foroni, 2011, American journal of hematology.

Technical aspects and clinical applications of measuring BCR‐ABL1 transcripts number in chronic myeloid leukemia

Letizia Foroni, John Goldman, D. Marin, 2009, American journal of hematology.

Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.

M. de Boer, D. Roos, R. van Zwieten, 2002, Blood.

Fast‐mode duplex qPCR for BCR‐ABL1 molecular monitoring: Innovation, automation, and harmonization

N. Cross, H. White, L. Foroni, 2012, American journal of hematology.

haploinsufficiency congenita and aplastic anemia reduce telomerase activity via Heterozygous telomerase RNA mutations found in dyskeratosis

T. Vulliamy, P. Mason, I. Dokal, 2013 .

Fast‐mode duplex qPCR for BCR‐ABL1 molecular monitoring: Innovation, automation, and harmonization

N. Cross, H. White, L. Foroni, 2012, American journal of hematology.