Transient monosomy 7: A case series in children and review of the literature

Cancer

Volumn 85, Issue 12, 1999, Pages 2655-2661

  Mantadakis, Elpis ^a   Shannon, Kevin M ^b   Singer, Dale Anne ^c   Finklestein, Jerry ^d   Chan, Ka Wah ^e   Hilden, Joanne M ^f   Sandler, Eric S ^g  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c PHOENIX CHILDREN'S HOSPITAL   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF TEXAS   (United States)

^f UNIVERSITY OF MINNESOTA   (United States)

^g NEMOURS CHILDREN S CLINIC   (United States)

Author keywords

Cytogenetics; Fluorescent in situ hybridization (FISH); Monosomy 7; Myelodysplastic syndromes (MDS); Spontaneous remission

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 7Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CYTOGENETICS; DISEASE ASSOCIATION; DISEASE COURSE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INFANT; MALE; MONOSOMY 7; MYELODYSPLASTIC SYNDROME; PREDICTION; PRIORITY JOURNAL; REMISSION;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 7; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MONOSOMY; MYELODYSPLASTIC SYNDROMES; PROGNOSIS; REMISSION, SPONTANEOUS;

EID: 0033564105     PISSN: 0008543X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0142(19990615)85:12<2655::AID-CNCR23>3.0.CO;2-W     Document Type: Article

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