Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.

McDonell, N; Ramser, J; Francis, F; Vinet, M C; Rider, S; Sudbrak, R; Riesselman, L; Yaspo, M L; Reinhardt, R; Monaco, A P; Ross, F; Kahn, A; Kearney, L; Buckle, V; Chelly, J

McDonell, N; Ramser, J; Francis, F; Vinet, M C; Rider, S; Sudbrak, R; Riesselman, L; Yaspo, M L; Reinhardt, R; Monaco, A P; Ross, F; Kahn, A; Kearney, L; Buckle, V; Chelly, J.

Affiliation

McDonell N; Institut Cochin de Génétique Moléculaire, INSERM Unité 129, CHU Cochin-Port-Royal, 24 Rue du Faubourg Saint Jacques, Paris, 75014, France.

Genomics ; 64(3): 221-9, 2000 Mar 15.

Article in En | MEDLINE | ID: mdl-10756090

Subject(s)

Chromosome Breakage; Leukemia, Myeloid/genetics; Preleukemia/genetics; Sex Chromosome Aberrations/genetics; X Chromosome; Acute Disease; Aged; Blotting, Southern; Centromere; Chromosomes, Artificial, Yeast; Chromosomes, Bacterial; Cloning, Molecular; Contig Mapping; Cosmids; Expressed Sequence Tags; Female; Gene Duplication; Humans; In Situ Hybridization, Fluorescence; Long Interspersed Nucleotide Elements; Molecular Sequence Data; Myelodysplastic Syndromes/genetics; Sequence Analysis, DNA

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Collection: 01-internacional Database: MEDLINE Main subject: Preleukemia / Sex Chromosome Aberrations / X Chromosome / Leukemia, Myeloid / Chromosome Breakage Type of study: Risk_factors_studies Limits: Aged / Female / Humans Language: En Journal: Genomics Journal subject: GENETICA Year: 2000 Document type: Article Affiliation country: France Country of publication: United States

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