The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells
about
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaClinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach.Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type ICharacteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesisCongenital dyserythropoietic anaemias: new acquisitionsInherited hematological disorders due to defects in coat protein (COP)II complex.Hereditary red cell membrane disorders and laboratory diagnostic testing.Congenital dyserythropoietic anemias: molecular insights and diagnostic approachDiagnosis and management of congenital dyserythropoietic anemias.Gene Therapy with Hematopoietic Stem Cells: The Diseased Bone Marrow's Point of View.Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlations.Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene.[Hemoglobin disorders].Congenital dyserythropoietic anemia type I: report of a case.Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.Innovations Needed for Effective Implementation of Ex Vivo Gene Therapies.A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain.Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.Diagnosis and Management of Congenital Dyserythropoietic Anaemia Type II in a Secundigravida.Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.
P2860
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P2860
The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells
description
2010 nî lūn-bûn
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2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
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2010年論文
@zh-tw
2010年论文
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name
The morphological diagnosis of ...... al blood and bone marrow cells
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The morphological diagnosis of ...... al blood and bone marrow cells
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type
label
The morphological diagnosis of ...... al blood and bone marrow cells
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The morphological diagnosis of ...... al blood and bone marrow cells
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prefLabel
The morphological diagnosis of ...... al blood and bone marrow cells
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The morphological diagnosis of ...... al blood and bone marrow cells
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P2093
P2860
P1433
P1476
The morphological diagnosis of ...... al blood and bone marrow cells
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P2093
Hermann Heimpel
Josef Högel
Kerstin Kellermann
Klaus Schwarz
Nadine Neuschwander
P2860
P304
P356
10.3324/HAEMATOL.2009.014563
P577
2010-04-26T00:00:00Z