RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome

Virchows Archiv

Volumn 454, Issue 3, 2009, Pages 311-316

  Roberti, Maria Cristina ^a   La Starza, Roberta ^b   Surace, Cecilia ^a   Sirleto, Pietro ^a   Pinto, Rita Maria ^a   Pierini, Valentina ^b   Crescenzi, Barbara ^b   Mecucci, Cristina ^b   Angioni, Adriano ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b UNIVERSITY OF PERUGIA   (Italy)

Author keywords

Acute myeloid leukemia; Klinefelter syndrome

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; BONE MARROW CELL; BONE MARROW TRANSPLANTATION; CASE REPORT; CHILD; CLINICAL FEATURE; COLONY FORMING UNIT GEMM; CYTOGENETICS; ERYTHROID CELL; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE REARRANGEMENT; GENETIC TRAIT; HUMAN; HUMAN TISSUE; KLINEFELTER SYNDROME; LABORATORY TEST; MALE; MEGAKARYOCYTE; MOLECULAR MECHANICS; PRESCHOOL CHILD; PRIORITY JOURNAL; RABGAP1L GENE; THROMBOCYTOPENIA; TRISOMY; TUMOR GENE; Y CHROMOSOME;

CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, Y; GENE REARRANGEMENT; GTPASE-ACTIVATING PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KLINEFELTER SYNDROME; LEUKEMIA, MYELOID, ACUTE; MALE; NERVE TISSUE PROTEINS;

EID: 67349160729     PISSN: 09456317     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00428-009-0732-z     Document Type: Article

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