FGFR3 gene mutations associated with human skeletal disorders occur rarely in multiple myeloma [11]

Blood

Volumn 92, Issue 8, 1998, Pages 2987-2989

  Fracchiolla, N S ^a   Luminari, S ^a   Baldini, L ^a   Lombardi, L ^a   Maiolo, A T ^a   Neri, A ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ACHONDROPLASIA; BONE DYSPLASIA; CONTROLLED STUDY; DISEASE ASSOCIATION; GENE MUTATION; HUMAN; HUMAN CELL; HYPOCHONDROPLASIA; LETTER; MAJOR CLINICAL STUDY; MULTIPLE MYELOMA; PLASMA CELL LEUKEMIA; PRIORITY JOURNAL;

EID: 0032532626     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.8.2987     Document Type: Letter

References (15)