- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
In: Science (1989) 244, 1575-1578.
- Classification
-
Biowissenschaften, Biologie
- Keyword
-
Histologie
Cytologie
- Event
-
Veröffentlichung
- (where)
-
Würzburg
- (who)
-
Universität Würzburg
- (when)
-
2009
- Creator
-
Gessler, Manfred
SIMOLA, KALLE O.
Bruns, Gail A. P.
- URN
-
urn:nbn:de:bvb:20-opus-30177
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:46 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Gessler, Manfred
- SIMOLA, KALLE O.
- Bruns, Gail A. P.
- Universität Würzburg
Time of origin
- 2009
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Systematic cloning and functional analysis of the proteins encoded on human chromosome 21
Molecular characterisation of the rare translocation t(5;11)(q31;q23) identifies a novel MLL partner gene : a candidate tumor suppressor gene of acute myeologenous leukemia on chromosome 5q31
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome
Molecular characterization of a chromosome 1;22 translocation in a patient with a phenotype resembling Costello syndrome
Molecular characterization of a chromosome 1;22 translocation in a patient with a phenotype resembling Costello syndrome
The Economics of Human Cloning
Pathways of nucleocytoplasmic translocation of ribonucleoproteins
Chromosome structure and the stability of chromosome ends in Streptomyces
Functional consequences of chromosome holocentricity
Molecular biology of chromosome function
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Chromosome painting and arrangement of interphase chromosome territories in Arabidopsis thaliana
Systematic cloning and functional analysis of the proteins encoded on human chromosome 21
Molecular characterisation of the rare translocation t(5;11)(q31;q23) identifies a novel MLL partner gene : a candidate tumor suppressor gene of acute myeologenous leukemia on chromosome 5q31
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome
Molecular characterization of a chromosome 1;22 translocation in a patient with a phenotype resembling Costello syndrome
Molecular characterization of a chromosome 1;22 translocation in a patient with a phenotype resembling Costello syndrome
The Economics of Human Cloning
Pathways of nucleocytoplasmic translocation of ribonucleoproteins
Chromosome structure and the stability of chromosome ends in Streptomyces
Functional consequences of chromosome holocentricity
Molecular biology of chromosome function
Translocation