Absence of mutation at the GAP-related domain of the neurofibromatosis type 1 gene in sporadic neurofibrosarcomas and other bone and soft tissue sarcomas.

Gómez, L; Barrios, C; Kreicbergs, A; Zetterberg, A; Pestaña, A; Castresana, J S

Gómez, L; Barrios, C; Kreicbergs, A; Zetterberg, A; Pestaña, A; Castresana, J S.

Affiliation

Gómez L; Instituto de Investigaciones Biomédicas, CSIC, Madrid, Spain.

Cancer Genet Cytogenet ; 81(2): 173-4, 1995 Jun.

Article in En | MEDLINE | ID: mdl-7621416

Subject(s)

Bone Neoplasms/genetics; Neurofibromatosis 1/genetics; Neurofibrosarcoma/genetics; Proteins/genetics; Sarcoma/genetics; Soft Tissue Neoplasms/genetics; DNA Mutational Analysis; Humans; Neurofibromin 1; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational

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Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Soft Tissue Neoplasms / Bone Neoplasms / Proteins / Neurofibromatosis 1 / Neurofibrosarcoma Limits: Humans Language: En Journal: Cancer Genet Cytogenet Year: 1995 Document type: Article Affiliation country: Spain Country of publication: United States

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