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Refinado por: assunto: Adult remover Base de dados/Biblioteca: Wiley-Blackwell Full Collection 2009 remover
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1
The incidences of trisomy 8, trisomy 9 and D20S108 deletion in polycythaemia vera: an analysis of blood granulocytes using interphase fluorescence in situ hybridization
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The incidences of trisomy 8, trisomy 9 and D20S108 deletion in polycythaemia vera: an analysis of blood granulocytes using interphase fluorescence in situ hybridization

Westwood, N. B. ; Gruszka‐Westwood, A. M. ; Pearson, C. E. ; DeLord, C. F. M. ; Green, A. R. ; Huntly, B. J. P. ; Lakhani, A. ; McMullin, M. F. ; Pearson, T. C.

British journal of haematology, 2000-09, Vol.110 (4), p.839-846 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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2
Mutation and methylation analysis of the transforming growth factor β receptor II gene in polycythaemia vera
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Mutation and methylation analysis of the transforming growth factor β receptor II gene in polycythaemia vera

Li, Juan ; Bench, Anthony J. ; Huntly, Brian J. P. ; Green, Anthony R.

British journal of haematology, 2001-12, Vol.115 (4), p.872-880 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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3
Does isochromosome 7q mandate bone marrow transplant in children with Shwachman–Diamond syndrome?
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Does isochromosome 7q mandate bone marrow transplant in children with Shwachman–Diamond syndrome?

Cunningham, Joan ; Sales, Mark ; Pearce, Andrew ; Howard, Julie ; Stallings, Ray ; Telford, Nicholas ; Wilkie, Rosalie ; Huntly, Brian ; Thomas, Angela ; O'Marcaigh, Aengus ; Will, Andrew ; Pratt, Norman

British journal of haematology, 2002-12, Vol.119 (4), p.1062-1069 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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