Evidence for genetic homogeneity in a familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML) [8]

Blood

Volumn 92, Issue 7, 1998, Pages 2600-2601

  Arepally, G ^a   Rebbeck, T R ^a   Song, W ^a   Gilliland, G ^a   Maris, J M ^a   Poncz, M ^a  

^a UNIVERSITY OF NEW MEXICO HEALTH SCIENCES CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 21Q; DISEASE PREDISPOSITION; FAMILY STUDY; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUMAN TISSUE; IDIOPATHIC THROMBOCYTOPENIC PURPURA; LETTER; MALE; PEDIGREE; PRIORITY JOURNAL; RISK ASSESSMENT; RISK FACTOR;

EID: 0032189080     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.7.2600     Document Type: Letter

References (8)