T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6

Pediatric Blood and Cancer

Volumn 55, Issue 4, 2010, Pages 722-724

  Chao, Mwe Mwe ^a   Todd, Matthew A ^b   Kontny, Udo ^c   Neas, Katherine ^d   Sullivan, Michael J ^e   Hunter, Alasdair G ^f   Picketts, David J ^b   Kratz, Christian P ^g  

^a CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^b OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

^c UNIVERSITY OF FREIBURG   (Germany)

^d CAPITAL AND COAST DISTRICT HEALTH BOARD   (New Zealand)

^e UNIVERSITY OF OTAGO   (New Zealand)

^f CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^g NATIONAL CANCER INSTITUTE   (United States)

Author keywords

B rjeson Forssman Lehmann syndrome; PHF6; T cell ALL lymphoma

Indexed keywords

ANTINEOPLASTIC AGENT; CD2 ANTIGEN; CD3 ANTIGEN; CD4 ANTIGEN; CD45 ANTIGEN; CD5 ANTIGEN; CD7 ANTIGEN; CD9 ANTIGEN; FANCONI ANEMIA GROUP L PROTEIN; T6 ANTIGEN; CARRIER PROTEIN; PHF6 PROTEIN, HUMAN;

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; BONE MARROW CELL; BORJESON FORSSMAN LEHMANN SYNDROME; CANCER CHEMOTHERAPY; CANCER SUSCEPTIBILITY; CASE REPORT; CHILD; CODON; DISEASE ASSOCIATION; DNA EXTRACTION; EXON; FLOW CYTOMETRY; GENE MUTATION; GENE OVEREXPRESSION; GYNECOMASTIA; HUMAN; HUMAN CELL; LEUKEMIA CELL; LEUKOCYTOSIS; LIVER FAILURE; LYMPH NODE; MALE; NUCLEAR LOCALIZATION SIGNAL; OBESITY; OUTCOME ASSESSMENT; PRIORITY JOURNAL; SCHOOL CHILD; T CELL LYMPHOMA; T LYMPHOCYTE; X CHROMOSOME; X CHROMOSOME LINKED DISORDER; ZINC FINGER MOTIF; GENETICS; MUTATION; X LINKED MENTAL RETARDATION;

CARRIER PROTEINS; CHILD; HUMANS; MALE; MENTAL RETARDATION, X-LINKED; MUTATION; PRECURSOR T-CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;

EID: 77957078794     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.22574     Document Type: Article

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