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Gewählte Publikation:

Taniwaki, M; Speicher, MR; Lengauer, C; Jauch, A; Popp, S; Cremer, T.
Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization.
Cancer Genet Cytogenet. 1993; 70(2):99-102 Doi: 10.1016/0165-4608(93)90175-L (- Case Report) [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Speicher Michael
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Abstract:
A patient with acute nonlymphocytic leukemia (ANLL), M5b according to French-American-British (FAB) classification, showed monosomy 16, an extra 1p-, and a 21q+. These derivative chromosomes could not be defined by GTG-banding. For better characterization, we performed two-color fluorescence in situ hybridization (FISH) experiments applying DNA libraries from sorted human chromosomes, chromosome-specific repetitive probes, and a band-specific YAC-clone. With these FISH studies the karyotype could be characterized as 46,XY, +der(1)t(1;21)(p11;?), -16,der(21)t(16;21) (p11.1;q22).
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Chromosome Aberrations -
Chromosome Banding -
Chromosomes, Artificial, Yeast -
Chromosomes, Human, Pair 1 -
Chromosomes, Human, Pair 16 -
Chromosomes, Human, Pair 21 -
DNA Probes -
Gene Library -
Genetic Markers -
Humans -
In Situ Hybridization, Fluorescence -
Karyotyping -
Leukemia, Nonlymphocytic, Acute - genetics
Male - genetics
Monosomy - genetics
Translocation, Genetic - genetics

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