t(11;22)(q23;q11.2) in acute myeloid leukemia of infant twins fuses MLL with hCDCrel, a cell division cycle gene in the genomic region of deletion in DiGeorge and velocardiofacial syndromes

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 11, 1998, Pages 6415-6418

  Megonigal, Maureen D ^a   Rappaport, Eric F ^a   Jones, Douglas H ^c   Williams, Terence M ^a   Lovett, Brian D ^a   Kelly, Kara M ^d   Lerou, Paul H ^e   Moulton, Thomas ^d   Budarf, Marcia L ^a,b   Felix, Carolyn A ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c UNIVERSITY OF IOWA   (United States)

^d Columbia Univ Coll Phys Surgs ^*  (United States)

^e THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; CASE REPORT; CELL DIVISION; CHROMOSOME TRANSLOCATION; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; GENE REARRANGEMENT; HUMAN; HUMAN CELL; INFANT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TWINS; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ACUTE DISEASE; BASE SEQUENCE; CELL CYCLE PROTEINS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DISEASES IN TWINS; DNA-BINDING PROTEINS; FACE; GENE DELETION; GENOME, HUMAN; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; LEUKEMIA, MYELOID; MOLECULAR SEQUENCE DATA; MYELOID-LYMPHOID LEUKEMIA PROTEIN; PROTO-ONCOGENES; SYNDROME; TRANSCRIPTION FACTORS; TRANSLOCATION, GENETIC; TWINS;

EID: 11544323440     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.11.6413     Document Type: Article

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