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Human Genetics|November 1, 1979
Sister chromatid exchange in cell lines from malignant lymphomas (lymphoma lines)C Fonatsch, M Schaadt, V DiehlBritish Journal of Haematology|May 1, 1985
Persistent Epstein-Barr virus infection associated with monosomy 7 or chromosome 3 abnormality in childhood myeloproliferative disordersB Stollmann, C Fonatsch, W HaversLeukemia|August 1, 1994
Correlation of cytogenetic findings with clinical features in 18 patients with inv(3)(q21q26) or t(3;3)(q21;q26)C Fonatsch, H Gudat, E Lengfelder, et al.Human Genetics|January 1, 1984
Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseasesB Schulze, C Golinski, C FonatschCytogenetics 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----p23.05A Volz, C Fonatsch, A ZieglerClinical Genetics|February 1, 1979
Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomesC Fonatsch, S D Flatz, E WeitzelHuman Genetics|September 2, 1979
Frequency of sister chromatid exchanges in a balanced reciprocal whole-arm translocationA M Schober, C Fonatsch, O SchoberDer Urologe. Ausg. A|January 1, 1980
[Transvesical sonography of the seminal vesicles (author's transl)]M Gerken, A Grote, F HildCancer Genetics and Cytogenetics|June 1, 1987
Translocation (6;9)(p23;q34) in smoldering leukemia and acute nonlymphocytic leukemiaC Fonatsch, B Stollmann, J Holldack, et al.Leukemia|August 1, 1996
Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factorC Schoch, D Haase, T Haferlach, et al.Pageof 82