UNSMAKING PRIMARY IMMUNE DEFICIENCIES IN EARLY-ONSET EVANS SYNDROME ă USING IMMUNOPHENOTYPING AND NGS: TOWARDS A CLINICAL AND GENETIC ă CLASSIFICATION - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Haematologica Année : 2016

UNSMAKING PRIMARY IMMUNE DEFICIENCIES IN EARLY-ONSET EVANS SYNDROME ă USING IMMUNOPHENOTYPING AND NGS: TOWARDS A CLINICAL AND GENETIC ă CLASSIFICATION

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hal-01482533 , version 1 (03-03-2017)

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  • HAL Id : hal-01482533 , version 1

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F. Rieux-Laucat, N. Aladjidi, C. Picard, H. Fernandes, Yves Bertrand, et al.. UNSMAKING PRIMARY IMMUNE DEFICIENCIES IN EARLY-ONSET EVANS SYNDROME ă USING IMMUNOPHENOTYPING AND NGS: TOWARDS A CLINICAL AND GENETIC ă CLASSIFICATION. Haematologica, 2016, 101 (1), pp.302. ⟨hal-01482533⟩
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