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Annals of Hematology|April 1, 1995
Cytogenetic findings in 179 patients with myelodysplastic syndromesD Haase, C Fonatsch, M Freund, et al.
British Journal of Haematology|September 1, 1996
Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t(15;17)(q22;q21): a report on 50 patientsC Schoch, D Haase, T Haferlach, et al.
Human Genetics|January 1, 1983
Frequency of fragile X chromosomes, fra(X), in lymphocytes in relation to blood storage time and culture techniquesC Fonatsch, E Schwinger
Blut|March 1, 1990
Karyotype and in vitro-response to GM-CSF. Analysis of bone marrow cultures in leukemia, myelodysplasia and aplastic anemiaD Haase, C Fonatsch
Onkologie|August 1, 1987
[Chromosome aberrations and malignant lymphomas]C Fonatsch, G Gradl
Wiener Klinische Wochenschrift|April 16, 1982
[Fragile X chromosome and X-linked mental retardation (author's transl)]C Fonatsch, S D Flatz
Humangenetik|June 19, 1975
De novo (11;13) translocationC Fonatsch, S D Flatz
British Journal of Haematology|July 1, 1989
Recombinant human interferon (IFN) alpha-2b in chronic myelogenous leukaemia: dose dependency of response and frequency of neutralizing anti-interferon antibodiesM Freund, P von Wussow, H Diedrich, et al.
Human Genetics|June 27, 1978
Balanced reciprocal whole-arm translocation t(1;19) in three generationsA M Schober, C Fonatsch
In Vivo (Athens, Greece)|May 1, 1991
Rearrangements of immunoglobulin- and BCR-genes in chronic myeloid leukemiaH Tesch, C Fonatsch, V Diehl
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