Complex chromosome abnormality mimicking t(8;21)in an acute myeloblastic leukemia.

Busson-Le Coniat, M; Daniel, M; Berger, R

Busson-Le Coniat, M; Daniel, M; Berger, R.

Affiliation

Busson-Le Coniat M; Unité Inserm U434, SD 401 No 434 CNRS, institut de génétique moléculaire, 27, rue Juliette-Dodu, 75010, Paris, France.

Ann Genet ; 44(1): 9-11, 2001.

Article in En | MEDLINE | ID: mdl-11334611

Subject(s)

Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 21; Chromosomes, Human, Pair 8; Leukemia, Myeloid, Acute/genetics; Translocation, Genetic; Adult; Chromosome Aberrations/genetics; Chromosome Mapping; Chromosomes, Human, Pair 7; Female; Humans; In Situ Hybridization, Fluorescence; Karyotyping

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 8 / Chromosomes, Human, Pair 21 / Leukemia, Myeloid, Acute / Chromosome Aberrations / Chromosome Disorders Limits: Adult / Female / Humans Language: En Journal: Ann Genet Year: 2001 Document type: Article Affiliation country: France Country of publication: Netherlands

Search on Google

Add to My VHL

XML

PubMed Links