Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome

British Journal of Haematology

Volumn 145, Issue 4, 2009, Pages 533-534

  Steinemann, Doris ^a   Praulich, Inka ^a   Otto, Noreen ^a   Göhring, Gudrun ^a   Niemeyer, Charlotte M ^b   Schlegelberger, Brigitte ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b UNIVERSITY OF FREIBURG   (Germany)

Author keywords

Bone marrow failure; HAX1; MDS

Indexed keywords

ADOLESCENT; ADULT; APOPTOSIS; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA EXTRACTION; FEMALE; GENE; GENOTYPE; GRANULOCYTE; HAX1 GENE; HEMATOPOIETIC CELL; HUMAN; INFORMED CONSENT; LETTER; MALE; MALIGNANT TRANSFORMATION; MONONUCLEAR CELL; MUTATION; MYELODYSPLASTIC SYNDROME; NEUTROPENIA; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MYELODYSPLASTIC SYNDROMES; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS;

EID: 65349137591     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2009.07634.x     Document Type: Letter

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