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Volumn 7, Issue 1, 2001, Pages 67-71

Cytogenetic and histopathologic studies of congenital supratentorial primitive neuroectodermal tumors: A case report

Author keywords

Brain neoplasm; Congenital brain tumor; Cytogenetic studies; PNET; Primitive neuroectodermal tumor

Indexed keywords

ARTICLE; CASE REPORT; CENTRAL NERVOUS SYSTEM TUMOR; CHROMOSOME 17P; CHROMOSOME DELETION; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENETIC ANALYSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MALE; MEDULLOBLASTOMA; NEUROECTODERM TUMOR; NEWBORN; ONCOGENE C MYC; PATHOGENESIS;

EID: 0034950846     PISSN: 12194956     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF03032609     Document Type: Article
Times cited : (14)

References (30)
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  • 22
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    • High resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors (PNET) reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in band 17p11.2
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.