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Search Results - Henter, J.I
Search Results - Henter, J.I
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Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms
by
Tesi, B
,
Davidsson, J
,
Voss, M
,
Rahikkala, E
,
Holmes, T
,
Chiang, S
,
Komulainen-Ebrahim, J
,
Kokkonen, H
,
Bryder, D
,
Fioretos, T
,
Henter, J.I
,
Möttönen, M
,
Niinimäki, R
,
Nilsson, L
,
Pronk, C.J
,
Uusimaa, J
,
Moilanen, J
,
Tedgård, U
,
Cammenga, J
,
Bryceson, Y
Published in
Leukemia research
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Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden
by
Melin, M.
,
Entesarian, M.
,
Carlsson, G.
,
Garwicz, D.
,
Klein, C.
,
Fadeel, B.
,
Nordenskjöld, M.
,
Palmblad, J.
,
Henter, J.I.
,
Dahl, N.
Published in
Biochemical and biophysical research communications
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P02.05CLINICAL STUDY PHASE II WITH DENDRITIC CELL VACCINATION AND TUMOUR LYSATE AS ADD-ON THERAPY IN HIGH GRADE GLIOMA
by
Stragliotto, G.
,
Holm, S.
,
Adamson, L.
,
Giraud, G.
,
Henter, J.I.
Published in
Neuro-oncology (Charlottesville, Va.)
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21 - Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms
by
Tesi, B.
,
Davidsson, J.
,
Voss, M.
,
Rahikkala, E.
,
Holmes, T.
,
Chiang, S.
,
Komulainen-Ebrahim, J.
,
Kokkonen, H.
,
Bryder, D.
,
Fioretos, T.
,
Henter, J.I.
,
Möttönen, M.
,
Niinimäki, R.
,
Nilsson, L.
,
Pronk, C.J.
,
Uusimaa, J.
,
Moilanen, J.
,
Tedgård, U.
,
Cammenga, J.
,
Bryceson, Y.
Published in
Leukemia research
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Age-dependent differences in Nordic children with ITP
by
Rosthøj, S.
,
Hedlund-Treutiger, I.
,
Rajantie, J.
,
Zeller, B.
,
Jonsson, O.G.
,
Henter, J.I.
Published in
The Journal of pediatrics
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