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Chromosome 17 abnormalities and lack of TP53 mutations in paediatric central nervous system tumours.
Phelan, C M; Liu, L; Ruttledge, M H; Müntzning, K; Ridderheim, P A; Collins, V P.
Affiliation
  • Phelan CM; Ludwig Institute for Cancer Research, Karolinska Hospital, Stockholm, Sweden.
Hum Genet ; 96(6): 684-90, 1995 Dec.
Article in En | MEDLINE | ID: mdl-8522328
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Neoplasms / Chromosomes, Human, Pair 17 / Brain Neoplasms / Genes, p53 / Chromosome Aberrations / Chromosome Deletion / Chromosome Disorders / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Hum Genet Year: 1995 Document type: Article Affiliation country: Sweden Country of publication: Germany
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Neoplasms / Chromosomes, Human, Pair 17 / Brain Neoplasms / Genes, p53 / Chromosome Aberrations / Chromosome Deletion / Chromosome Disorders / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Hum Genet Year: 1995 Document type: Article Affiliation country: Sweden Country of publication: Germany