Genetic and molecular diagnosis of severe congenital neutropenia.
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SerpinB1 protects the mature neutrophil reserve in the bone marrowSevere congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis.A novel homozygous mutation in G6PC3 presenting as cyclic neutropenia and severe congenital neutropenia in the same family.Relationship between paediatric CT scans and subsequent risk of leukaemia and brain tumours: assessment of the impact of underlying conditions.Molecular mechanisms regulating NETosis in infection and disease.Neutropenia and primary immunodeficiency diseases.Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS.Hematopoietic stem cell transplantation for severe congenital neutropenia.Aggressive forms of periodontitis secondary to systemic disorders.Granulocyte colony-stimulating factor receptor mutations in myeloid malignancy.Genetic analysis and clinical picture of severe congenital neutropenia in Israel.Spectrum of bone marrow failures of myeloid series: new report of neutropenic patients from a referral pediatric center in Iran.Clinical, Laboratory, and Molecular Characteristics and Remission Status in Children With Severe Congenital and Non-congenital Neutropenia
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P2860
Genetic and molecular diagnosis of severe congenital neutropenia.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on January 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
@cs
name
Genetic and molecular diagnosis of severe congenital neutropenia.
@en
Genetic and molecular diagnosis of severe congenital neutropenia.
@nl
type
label
Genetic and molecular diagnosis of severe congenital neutropenia.
@en
Genetic and molecular diagnosis of severe congenital neutropenia.
@nl
prefLabel
Genetic and molecular diagnosis of severe congenital neutropenia.
@en
Genetic and molecular diagnosis of severe congenital neutropenia.
@nl
P2860
P1476
Genetic and molecular diagnosis of severe congenital neutropenia
@en
P2093
David C Dale
P2860
P356
10.1097/MOH.0B013E32831952DE
P577
2009-01-01T00:00:00Z