Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the Groupe Francais de Cytogenetique Hematologique

Leukemia

Volumn 11, Issue 9, 1997, Pages 1478-1485

  Leonard C ^a   Huret, J L ^b  

^a BICÊTRE HOSPITAL   (France)

^b POITIERS UNIVERSITY HOSPITAL   (France)

Author keywords

Childhood; Chromosome anomalies; Congenital genetic diseases; FAB classification; Myelodysplasia; Prognosis

Indexed keywords

ANTINEOPLASTIC AGENT;

AGE; ARTICLE; CHEMOTHERAPY; CHILD; CHILDHOOD DISEASE; CHROMOSOME 19; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CYTOGENETICS; DISEASE CLASSIFICATION; FEMALE; FRANCE; HUMAN; HUMAN CELL; INFANT; KARYOTYPE; LYMPHOCYTE CLONE; MALE; MALFORMATION SYNDROME; MONOSOMY 7; MYELODYSPLASIA; MYELODYSPLASTIC SYNDROME; PRELEUKEMIA; PRIORITY JOURNAL; PROGNOSIS; RADIOTHERAPY; SEX DIFFERENCE; SURVIVAL TIME; TRISOMY; TRISOMY 8;

EID: 0030772564     PISSN: 08876924     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.leu.2400771     Document Type: Article

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