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Human Genetics
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November 1, 1979
Sister chromatid exchange in cell lines from malignant lymphomas (lymphoma lines)
C Fonatsch, M Schaadt, V Diehl
British Journal of Haematology
|
May 1, 1985
Persistent Epstein-Barr virus infection associated with monosomy 7 or chromosome 3 abnormality in childhood myeloproliferative disorders
B Stollmann, C Fonatsch, W Havers
Human Genetics
|
January 1, 1984
Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseases
B Schulze, C Golinski, C Fonatsch
Leukemia & Lymphoma
|
October 1, 1992
Karyotype instability in myelodysplastic syndromes--a specific step in pathogenesis preceding clonal chromosome anomalies
D Haase, C Fonatsch, M Freund
Cytogenetics and Cell Genetics
|
January 1, 1992
Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2----p23.05
A Volz, C Fonatsch, A Ziegler
Clinical Genetics
|
February 1, 1979
Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes
C Fonatsch, S D Flatz, E Weitzel
Human Genetics
|
September 2, 1979
Frequency of sister chromatid exchanges in a balanced reciprocal whole-arm translocation
A M Schober, C Fonatsch, O Schober
Cancer Genetics and Cytogenetics
|
June 1, 1987
Translocation (6;9)(p23;q34) in smoldering leukemia and acute nonlymphocytic leukemia
C Fonatsch, B Stollmann, J Holldack, et al.
Human Genetics
|
May 8, 2000
Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients
K Wimmer, M Eckart, H Rehder, et al.
Leukemia Research
|
January 1, 1990
Analysis of bcr rearrangements in primary (essential) thrombocythaemia
H Tesch, R Zankovich, C Fonatsch, et al.
Page
of 16
Search research articles
Search
Showing results (11-20 of 157) with videos related to
Sort By:
Page
of 16
Human Genetics
|
November 1, 1979
Sister chromatid exchange in cell lines from malignant lymphomas (lymphoma lines)
C Fonatsch, M Schaadt, V Diehl
British Journal of Haematology
|
May 1, 1985
Persistent Epstein-Barr virus infection associated with monosomy 7 or chromosome 3 abnormality in childhood myeloproliferative disorders
B Stollmann, C Fonatsch, W Havers
Human Genetics
|
January 1, 1984
Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseases
B Schulze, C Golinski, C Fonatsch
Leukemia & Lymphoma
|
October 1, 1992
Karyotype instability in myelodysplastic syndromes--a specific step in pathogenesis preceding clonal chromosome anomalies
D Haase, C Fonatsch, M Freund
Cytogenetics and Cell Genetics
|
January 1, 1992
Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2----p23.05
A Volz, C Fonatsch, A Ziegler
Clinical Genetics
|
February 1, 1979
Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes
C Fonatsch, S D Flatz, E Weitzel
Human Genetics
|
September 2, 1979
Frequency of sister chromatid exchanges in a balanced reciprocal whole-arm translocation
A M Schober, C Fonatsch, O Schober
Cancer Genetics and Cytogenetics
|
June 1, 1987
Translocation (6;9)(p23;q34) in smoldering leukemia and acute nonlymphocytic leukemia
C Fonatsch, B Stollmann, J Holldack, et al.
Human Genetics
|
May 8, 2000
Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients
K Wimmer, M Eckart, H Rehder, et al.
Leukemia Research
|
January 1, 1990
Analysis of bcr rearrangements in primary (essential) thrombocythaemia
H Tesch, R Zankovich, C Fonatsch, et al.
Page
of 16