Routine karyotyping in Wilms tumor

Cancer Genetics and Cytogenetics

Volumn 96, Issue 2, 1997, Pages 151-156

  Betts, David R ^a,c   Koesters, Robert ^b   Plüss, Hans Jörg ^a   Niggli, Felix K ^a  

^a Center for MR Research Children's Hospital Zürich   (Switzerland)

^b UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^c Kinderspital Zürich ^*  (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 12; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 1Q; CHROMOSOME 6; CHROMOSOME 7; CHROMOSOME 8; CHROMOSOME 8Q; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME MOSAICISM; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; KARYOTYPING; MALE; NEEDLE BIOPSY; NEPHROBLASTOMA; NUMERICAL CHROMOSOME ABERRATION; PRIORITY JOURNAL; STRUCTURAL CHROMOSOME ABERRATION; TRISOMY 18;

ANIMALS; BIOPSY, NEEDLE; CHILD; CHILD, PRESCHOOL; CHROMOSOME BANDING; DNA-BINDING PROTEINS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; MICE; MICE, NUDE; NEOPLASM TRANSPLANTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; TRANSCRIPTION FACTORS; WILMS TUMOR; WT1 PROTEINS;

MUS MUSCULUS;

EID: 0030855125     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00318-4     Document Type: Article

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