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Acta Neurochirurgica. Supplement
|
January 1, 1996
Correlation between cytogenetic and clinical findings in 215 human meningiomas
W I Steudel, R Feld, W Henn, et al.
Cancer Genetics and Cytogenetics
|
November 7, 2000
Comparative genomic hybridization reveals recurrent enhancements on chromosome 20 and in one case combined amplification sites on 15q24q26 and 20p11p12 in glioblastomas
C Brunner, V Jung, W Henn, et al.
Human Genetics
|
May 1, 1993
Immunophenotyping of mitotic cells from long-term cultures of chorionic villi
N Zimmer, E Göttert, J Kraus, et al.
Human Genetics
|
March 1, 1992
Search for putative suppressor genes in meningioma: significance of chromosome 22
G Schneider, S Lutz, W Henn, et al.
Anticancer Research
|
May 1, 1989
Differential activity of two oncogenes from chromosome #7 in human glioblastoma cell lines
E Göttert, W Henn, B Theisinger, et al.
Human Genetics
|
October 1, 1990
In situ chromosome preparation technique for simultaneous cytogenetic and immunocytochemical studies on cell cultures of solid tumors
W Henn, J Lehr, G Unteregger, et al.
Neuropathology and Applied Neurobiology
|
October 1, 1994
Detection of numerical chromosome aberrations in brain tumours by fluorescence in situ hybridization on smear preparations of small tumour biopsies
M Löw, W Feiden, J R Moringlane, et al.
Nucleic Acids Research
|
September 12, 1989
A polymorphic DNA probe from chromosome 19 (19cen-q11)
R Metzdorf, E Göttert, W Henn, et al.
American Journal of Medical Genetics
|
September 20, 2000
Lung hypoplasia in a patient with del(2)(q33-q35) demonstrated by chromosome microdissection
B W Kramer, T Martin, W Henn, et al.
Clinical Genetics
|
November 1, 1991
Mosaic tetraploidy in a liveborn infant with features of the DiGeorge anomaly
B Wullich, W Henn, E Groterath, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 84) with videos related to
Sort By:
Page
of 9
Acta Neurochirurgica. Supplement
|
January 1, 1996
Correlation between cytogenetic and clinical findings in 215 human meningiomas
W I Steudel, R Feld, W Henn, et al.
Cancer Genetics and Cytogenetics
|
November 7, 2000
Comparative genomic hybridization reveals recurrent enhancements on chromosome 20 and in one case combined amplification sites on 15q24q26 and 20p11p12 in glioblastomas
C Brunner, V Jung, W Henn, et al.
Human Genetics
|
May 1, 1993
Immunophenotyping of mitotic cells from long-term cultures of chorionic villi
N Zimmer, E Göttert, J Kraus, et al.
Human Genetics
|
March 1, 1992
Search for putative suppressor genes in meningioma: significance of chromosome 22
G Schneider, S Lutz, W Henn, et al.
Anticancer Research
|
May 1, 1989
Differential activity of two oncogenes from chromosome #7 in human glioblastoma cell lines
E Göttert, W Henn, B Theisinger, et al.
Human Genetics
|
October 1, 1990
In situ chromosome preparation technique for simultaneous cytogenetic and immunocytochemical studies on cell cultures of solid tumors
W Henn, J Lehr, G Unteregger, et al.
Neuropathology and Applied Neurobiology
|
October 1, 1994
Detection of numerical chromosome aberrations in brain tumours by fluorescence in situ hybridization on smear preparations of small tumour biopsies
M Löw, W Feiden, J R Moringlane, et al.
Nucleic Acids Research
|
September 12, 1989
A polymorphic DNA probe from chromosome 19 (19cen-q11)
R Metzdorf, E Göttert, W Henn, et al.
American Journal of Medical Genetics
|
September 20, 2000
Lung hypoplasia in a patient with del(2)(q33-q35) demonstrated by chromosome microdissection
B W Kramer, T Martin, W Henn, et al.
Clinical Genetics
|
November 1, 1991
Mosaic tetraploidy in a liveborn infant with features of the DiGeorge anomaly
B Wullich, W Henn, E Groterath, et al.
Page
of 9