-
1دورية أكاديمية
المساهمون: UCL - MD/BICL - Département de biochimie et de biologie cellulaire, UCL - MD/MNOP - Département de morphologie normale et pathologique, UCL - (SLuc) Service d'anatomie pathologique, UCL - (SLuc) Centre de malformations vasculaires congénitales, UCL - (SLuc) Centre de génétique médicale UCL
المصدر: Neuropathology and applied neurobiology, Vol. 29, no. 5, p. 462-471 (2003)
مصطلحات موضوعية: Central Nervous System Neoplasms, Chromosomes, Human, Pair 1, Pair 19, Pair 9, Gene Deletion, Genes, p16, Glioma, Humans, Loss of Heterozygosity, Methylation, Microsatellite Repeats, Necrosis, Oligodendroglioma, Polymerase Chain Reaction, Polymorphism, Single-Stranded Conformational, Promoter Regions (Genetics), Angiogenesis, CDKN2A, Deletion, Genetic, Microvascular proliferation, Mutation, Oligendroglioma
العلاقة: boreal:9633; http://hdl.handle.net/2078Test.1/9633; info:pmid/14507338; urn:ISSN:0305-1846; urn:EISSN:1365-2990
-
2مورد إلكتروني
المصدر: Neuropathology and applied neurobiology, Vol. 29, no. 5, p. 462-471 (2003)
مصطلحات الفهرس: Central Nervous System Neoplasms, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 9, Gene Deletion, Genes, p16, Glioma, Humans, Loss of Heterozygosity, Methylation, Microsatellite Repeats, Necrosis, Oligodendroglioma, Polymerase Chain Reaction, Polymorphism, Single-Stranded Conformational, Promoter Regions (Genetics), Angiogenesis, CDKN2A, Deletion, Genetic, Microvascular proliferation, Mutation, Oligendroglioma, info:eu-repo/semantics/article
URL:
http://hdl.handle.net/2078Test.1/9633