Search Results - "Reid, C.D.L."

Fluorescence in Situ Hybridization Analysis of t(3; 12)(q26;p13): A Recurring Chromosomal Abnormality Involving the TEL Gene (ETV6) in Myelodysplastic Syndromes by Raynaud, S.D., Baens, M., Grosgeorge, J., Rodgers, K., Reid, C.D.L., Dainton, M., Dyer, M., Fuzibet, J.G., Gratecos, N., Taillan, B., Ayraud, N., Marynen, P.

“…We have identified a new recurrent reciprocal translocation between chromosome 3 and 12 with breakpoints at bands 3q26 and 12p13, t(3; 12)(q26;p13) in the…”
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The significance of endogenous erythroid colonies (EEC) in haematological disorders by Reid, C D

“…The myeloproliferative disorders are the result of an underlying abnormality of the pluripotential stem cell. One feature of this abnormality is a greatly…”
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Correction by erythropoietin of anaemia in autonomic failure by Anand, P, Chen, F E, Reid, C D, Cotes, P M, Rudge, P, Coates, M

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Ranitidine fails to suppress the growth in vitro of haemopoietic progenitors from human peripheral blood or bone marrow by Reid, C D, Kirk, A

“…Ranitidine was added in various concentrations (25-1600 ng/ml) to clonal assays of haemopoietic progenitors of normal human peripheral blood or bone marrow…”
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Clinics in Haematology. Vol. 15, no. 1, Feb. 1986. Autologous Bone Marrow Transplantation by Reid, C.D.L.

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