A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21

Cancer Genetics and Cytogenetics

Volumn 156, Issue 1, 2005, Pages 62-67

  Hu, Jie ^a,b,c   Shekhter Levin, Sofia ^a,b,d,e   Shaw, Peter H ^f   Bay, Carolyn ^f   Kochmar, Sally ^a   Surti, Urvashi ^a,b,c,d,e  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF PITTSBURGH   (United States)

^d UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^e UNIVERSITY OF PITTSBURGH CANCER INSTITUTE   (United States)

^f CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; FEMALE; HUMAN; KARYOTYPE 46,XX; LABORATORY TEST; MONOSOMY 7; MOSAICISM; MYELODYSPLASTIC SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; TRISOMY 21;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 7; DOWN SYNDROME; FEMALE; HUMANS; KARYOTYPING; MONOSOMY; MOSAICISM; MYELODYSPLASTIC SYNDROMES; TRANSLOCATION, GENETIC;

EID: 10044280586     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2004.03.011     Document Type: Article

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