Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia

Pediatric Blood and Cancer

Volumn 51, Issue 2, 2008, Pages 171-177

  Rabin, Karen R ^a,b   Man, Tsz Kwong ^a   Yu, Alexander ^a   Folsom, Matthew R ^a   Zhao, Yi Jue ^a   Rao, Pulivarthi H ^a   Plon, Sharon E ^a   Naeem, Rizwan C ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TEXAS CHILDREN S CANCER CENTER   (United States)

Author keywords

Acute lymphoblastic leukemia (ALL); Array comparative genomic hybridization (aCGH)

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; BONE MARROW; CANCER DIAGNOSIS; CHILD; CHILDHOOD CANCER; CHROMOSOME 20Q; CHROMOSOME 9P; CHROMOSOME ABERRATION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MALE; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE; DIPLOIDY; GENETICS; INFANT; KARYOTYPING; LYMPHATIC LEUKEMIA; METHODOLOGY; NUCLEIC ACID HYBRIDIZATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; DIPLOIDY; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; NUCLEIC ACID HYBRIDIZATION; POLYMERASE CHAIN REACTION; PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;

EID: 45549092660     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.21488     Document Type: Article

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