hSNF5/INI1 inactivation is mainly associated with homozygous deletions and mitotic recombinations in rhabdoid tumors

Cancer Research

Volumn 59, Issue 13, 1999, Pages 3152-3156

  Rousseau Merck, Marie Françoise ^a   Versteege, Isabella ^a   Legrand, Isabelle ^a   Couturier, Jérôme ^a   Mairal, Aline ^a   Delattre, Olivier ^a   Aurias, Alain ^a  

^a INSTITUT CURIE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CELL LINE; CHROMOSOME 22Q; CHROMOSOME TRANSLOCATION; GENE DELETION; GENE INACTIVATION; GENE MUTATION; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; KARYOTYPE; PRIORITY JOURNAL; RHABDOID TUMOR; TUMOR SUPPRESSOR GENE;

CHROMOSOMAL PROTEINS, NON-HISTONE; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; CONSENSUS SEQUENCE; DNA-BINDING PROTEINS; GENE DELETION; GENES, TUMOR SUPPRESSOR; GENETIC MARKERS; HOMOZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICROSATELLITE REPEATS; MITOSIS; MUTATION; POLYMORPHISM, GENETIC; RECOMBINATION, GENETIC; RHABDOID TUMOR; TRANSCRIPTION FACTORS; TRANSLOCATION, GENETIC; TUMOR CELLS, CULTURED;

EID: 0033168062     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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