Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor.

Abrahamson, G M; Rack, K; Buckle, V J; Oscier, D G; Kelly, S; Wainscoat, J S

Abrahamson, G M; Rack, K; Buckle, V J; Oscier, D G; Kelly, S; Wainscoat, J S.

Affiliation

Abrahamson GM; Leukaemia Research Fund Molecular and Cytogenetic Haematology Unit, John Radcliffe Hospital, Headington, Oxford, U.K.

Cancer Genet Cytogenet ; 53(1): 91-5, 1991 May.

Article in En | MEDLINE | ID: mdl-2036643

Subject(s)

Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 7; ErbB Receptors/genetics; Gene Amplification; Hematologic Diseases/genetics; Translocation, Genetic; Aged; Female; Humans; Male; Middle Aged; Multiple Myeloma/genetics; Polycythemia Vera/genetics; Primary Myelofibrosis/genetics

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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 1 / Chromosomes, Human, Pair 7 / Gene Amplification / ErbB Receptors / Hematologic Diseases Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Cancer Genet Cytogenet Year: 1991 Type: Article Affiliation country: United kingdom

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