A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region.

Bench, A J; Aldred, M A; Humphray, S J; Champion, K M; Gilbert, J G; Asimakopoulos, F A; Deloukas, P; Gwilliam, R; Bentley, D R; Green, A R

Bench, A J; Aldred, M A; Humphray, S J; Champion, K M; Gilbert, J G; Asimakopoulos, F A; Deloukas, P; Gwilliam, R; Bentley, D R; Green, A R.

Affiliation

Bench AJ; Department of Haematology, University of Cambridge, United Kingdom.

Genomics ; 49(3): 351-62, 1998 May 01.

Article in En | MEDLINE | ID: mdl-9615219

Subject(s)

Chromosome Deletion; Chromosomes, Human, Pair 20; Myeloproliferative Disorders/genetics; Transcription, Genetic; Centromere; Chromosome Mapping; Chromosomes, Artificial, Yeast; DNA/blood; DNA/genetics; Family; Genetic Markers; Genotype; Granulocytes; Homozygote; Humans; Microsatellite Repeats; Polycythemia Vera/genetics; T-Lymphocytes

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Collection: 01-internacional Database: MEDLINE Main subject: Transcription, Genetic / Chromosomes, Human, Pair 20 / Chromosome Deletion / Myeloproliferative Disorders Limits: Humans Language: En Journal: Genomics Journal subject: GENETICA Year: 1998 Type: Article Affiliation country: United kingdom

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