Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis

British Journal of Haematology

Volumn 157, Issue 4, 2012, Pages 503-505

  Pressato, Barbara ^a   Valli, Roberto ^a   Marletta, Cristina ^a   Mare, Lydia ^a   Montalbano, Giuseppe ^a   Curto, Francesco Lo ^a   Pasquali, Francesco ^a   Maserati, Emanuela ^a  

^a UNIVERSITY OF INSUBRIA   (Italy)

Author keywords

Del(20); EIF6 gene; Shwachman Diamond syndrome

Indexed keywords

CELL PROTEIN; EIF6 PROTEIN; PROTEIN SBDS; UNCLASSIFIED DRUG;

BONE MARROW CELL; CELL CLONE; CHROMOSOME 20; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASE ASSOCIATION; EIF6 GENE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCATION; GENE LOSS; GENETIC RISK; HUMAN; LETTER; MICROARRAY ANALYSIS; MOLECULAR PATHOLOGY; PRIORITY JOURNAL; PROGNOSIS; PROTEIN LOCALIZATION; RISK ASSESSMENT; RISK FACTOR; SBDS GENE; SHWACHMAN SYNDROME;

BONE MARROW; BONE MARROW DISEASES; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 20; EUKARYOTIC INITIATION FACTORS; EXOCRINE PANCREATIC INSUFFICIENCY; HUMANS; LIPOMATOSIS; PROGNOSIS;

EID: 84859947806     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2012.09033.x     Document Type: Letter

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