Diamond-Blackfan anemia

Current Opinion in Pediatrics

Volumn 13, Issue 1, 2001, Pages 10-15

  Da Costa, Lydie ^a   Willig, Thiebaut Noel ^a   Fixler, Jason ^a   Mohandas, Narla ^a   Tchernia, Gil ^b  

^a LAWRENCE BERKELEY NATIONAL LABORATORY   (United States)

^b BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

RIBOSOME PROTEIN; RIBOSOME PROTEIN 19; STEROID; UNCLASSIFIED DRUG;

APLASTIC ANEMIA; BLACKFAN DIAMOND ANEMIA; CHROMOSOME 19; CHROMOSOME 8P; CLINICAL FEATURE; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; DISEASE SEVERITY; ERYTHROBLASTOPENIA; GENE MUTATION; GENETIC LINKAGE; HUMAN; INFANT; INHERITANCE; MOLECULAR GENETICS; PATHOGENESIS; PRIORITY JOURNAL; REVIEW; STEROID THERAPY; TREATMENT OUTCOME;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 8; FAILURE TO THRIVE; FANCONI ANEMIA; GENETIC HETEROGENEITY; HUMANS; INFANT; MUTATION;

EID: 0035136453     PISSN: 10408703     EISSN: None     Source Type: Journal    
DOI: 10.1097/00008480-200102000-00002     Document Type: Review

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