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Article

Narrowing the critical region for a rhabdoid tumor locus in 22q11

1 Jun 1996

Abstract excerpt

Rhabdoid tumor is a rare malignant neoplasm of childhood that may occur in various locations, including the central nervous system and the kidney. Previous cytogenetic studies of primary rhabdoid tumors have demonstrated monosomy or deletion of chromosome 22 and have implicated the presence of a rhabdoid tumor suppressor gene that maps to 22q. We have employed fluorescence in situ hybridization to narrow the...

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PMID: 8818656
DOI: 10.1002/(sici)1098-2264(199606)16:2<94::aid-gcc3>3.0.co;2-y

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