Chromosomal imbalances detected by comparative genomic hybridisation in atypical teratoid/rhabdoid tumours

Child's Nervous System

Volumn 20, Issue 4, 2004, Pages 221-224

  Rickert, Christian H ^a   Paulus, Werner ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

Author keywords

Brain; CGH; Chromosomal imbalances; Cytogenetics; Embryonal tumour; hSNF5 INI 1 monosomy

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 16P; CHROMOSOME 17P; CHROMOSOME 19; CHROMOSOME 20Q; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CHROMOSOME LOSS; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DATA ANALYSIS; DIAGNOSTIC TEST; DISEASE MARKER; FEASIBILITY STUDY; FEMALE; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; INFANT; MALE; MONOSOMY; NEWBORN; PRESCHOOL CHILD; PRIORITY JOURNAL; RHABDOID TUMOR; TERATOMA;

BRAIN NEOPLASMS; CHILD, PRESCHOOL; CHROMOSOMAL PROTEINS, NON-HISTONE; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 22; DNA-BINDING PROTEINS; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; NUCLEIC ACID HYBRIDIZATION; RHABDOID TUMOR; TRANSCRIPTION FACTORS;

EID: 2442718329     PISSN: 02567040     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00381-003-0909-8     Document Type: Article

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