Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene

Cancer Genetics and Cytogenetics

Volumn 92, Issue 1, 1997, Pages 73-78

  Watkins, David ^a   Ruttledge, Martin H ^a   Sarrazin, Julie ^a   Rangaratnam, Shyam ^a   Poisson, Michel ^b   Delattre, Jean Yves ^b   Rouleau, Guy A ^a  

^a MONTREAL GENERAL HOSPITAL   (Canada)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 22Q; GENE REPRESSION; GLIOMA; HUMAN; HUMAN TISSUE; NEUROFIBROMATOSIS; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

BRAIN NEOPLASMS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; GENE EXPRESSION REGULATION, NEOPLASTIC; GENES, NEUROFIBROMATOSIS 2; GENES, TUMOR SUPPRESSOR; GLIOMA; HUMANS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0030293102     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00149-5     Document Type: Article

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