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Search Results - Poddighe, P.J
Search Results - Poddighe, P.J
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Diffuse large B-cell lymphoma with MYC gene rearrangements
by
de Jonge, A.V
,
Roosma, T.J.A
,
Houtenbos, I
,
Vasmel, W.L.E
,
van de Hem, K
,
de Boer, J.P
,
van Maanen, T
,
Lindauer-van der Werf, G
,
Beeker, A
,
Timmers, G.J
,
Schaar, C.G
,
Soesan, M
,
Poddighe, P.J
,
de Jong, D
,
Chamuleau, M.E.D
Published in
European journal of cancer (1990)
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A novel cryptic CBFB-MYH11 gene fusion present at birth leading to acute myeloid leukemia and allowing molecular monitoring for minimal residual disease
by
Poddighe, P.J
,
Veening, M.A
,
Mansur, M.B
,
Loonen, A.H
,
Westers, T.M
,
Merle, P.A
,
Wessels, J.W
,
de Haas, V
,
Kors, W.A
,
Bhola, S.L
,
Wondergem, M.J
,
Ford, A.M
,
Kaspers, G.J.L
Published in
Human pathology : case reports
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Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A
by
Oegema, R.
,
de Klein, A.
,
Verkerk, A.J.
,
Schot, R.
,
Dumee, B.
,
Douben, H.
,
Eussen, B.
,
Dubbel, L.
,
Poddighe, P.J.
,
van der Laar, I.
,
Dobyns, W.B.
,
van der Spek, P.J.
,
Lequin, M.H.
,
de Coo, I.F.M.
,
de Wit, M.-C.Y.
,
Wessels, M.W.
,
Mancini, G.M.S.
Published in
Molecular syndromology
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European Journal Of Cancer
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Human Pathology : Case Reports
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Human Pathology. Case Reports
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Molecular Syndromology
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21Q2
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Aml
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Bcl-U
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Bcl2
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Cbfb-Myh11 Fusion Gene
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Chromosome 21
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Cytogenetics
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Da-Epoch-R
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Dlbcl
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Double Hit Lymphoma
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Dyrk1A
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Genetics & Heredity
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Hematology, Oncology And Palliative Medicine
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Life Sciences & Biomedicine
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Mental Retardation
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Microdeletion Syndrome
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Mrd
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Myc
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Neonatal Blood Spot
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Sciencedirect®
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Sciencedirect Freedom Collection 2022-2024
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Doaj Directory Of Open Access Journals
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