Rhnull syndrome: identification of a novel mutation in RHce

Rosa‚ KA; Reid‚ ME; Lomas-Francis‚ C.; Powell‚ VI; Costa‚ FF; Stinghen‚ ST; Watanabe‚ AM; Carboni‚ EK; Baldon‚ JP; Jucksch‚ MMF; others

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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Rhnull syndrome: identification of a novel mutation in RHce

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Author(s): Show less -	Rosa‚ KA ; Reid‚ ME ; Lomas-Francis‚ C. ; Powell‚ VI ; Costa‚ FF ; Stinghen‚ ST ; Watanabe‚ AM ; Carboni‚ EK ; Baldon‚ JP ; Jucksch‚ MMF ; others Total Authors: 11
Document type:	Journal article
Source:	Transfusion; v. 45, n. 11, p. 1796-1798, 2005.

FAPESP's process:	02/13801-7 - Hereditary hemoglobin disorders: molecular genetics, clinical features and animal models with the production of transgenic animals
Grantee:	Fernando Ferreira Costa
Support Opportunities:	Research Projects - Thematic Grants

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