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O A Haas

Showing results (11-20 of 201) with videos related to

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Cancer Genetics and Cytogenetics|October 15, 1993
Hypothesis: meiotic origin of trisomic neoplasmsO A Haas, M Seyger
Human Genetics|August 14, 2001
Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCRA Weinhäusel, O A Haas
American Journal of Hematology|January 1, 1988
Pure red cell aplasia as possible early manifestation of chronic myeloid leukemiaO A Haas, W Hinterberger, R Mörz
Journal of Medical Genetics|September 3, 2009
MECP2 mutation in one of Rett's original patientsM Freilinger, A Berndt, O A Haas
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer|January 1, 1993
Cytogenetic abnormalities associated with childhood acute myeloblastic leukemiaO A Haas, M Kronberger, L Mayerhofer
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Are ABL and BCR imprinted?M Fink, A Argyriou-Tirita, O A Haas
Klinische Padiatrie|July 1, 1986
[Guidelines for therapy of idiopathic thrombocytopenic purpura (ITP) in childhood]H Gadner, E R Grümayer, O A Haas
Nature|October 1, 1992
Parental origin of chromosomes involved in the translocation t(9;22)O A Haas, A Argyriou-Tirita, T Lion
Cancer Genetics and Cytogenetics|May 1, 1985
Noninvolvement of chromosome 16 in karyotype evolution of acute myeloid leukemia in a patient with a heritable fragile site on 16q22O A Haas, E Nacheva, J D Schwarzmeier
Cancer|November 1, 1987
Poorly differentiated, neuron-specific enolase positive round cell tumor with two translocations t(11;22) and t(21;22)O A Haas, A Chott, R Ladenstein, et al.
Pageof 21

Showing results (11-20 of 201) with videos related to

Sort By:
Pageof 21
Cancer Genetics and Cytogenetics|October 15, 1993
Hypothesis: meiotic origin of trisomic neoplasmsO A Haas, M Seyger
Human Genetics|August 14, 2001
Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCRA Weinhäusel, O A Haas
American Journal of Hematology|January 1, 1988
Pure red cell aplasia as possible early manifestation of chronic myeloid leukemiaO A Haas, W Hinterberger, R Mörz
Journal of Medical Genetics|September 3, 2009
MECP2 mutation in one of Rett's original patientsM Freilinger, A Berndt, O A Haas
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer|January 1, 1993
Cytogenetic abnormalities associated with childhood acute myeloblastic leukemiaO A Haas, M Kronberger, L Mayerhofer
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Are ABL and BCR imprinted?M Fink, A Argyriou-Tirita, O A Haas
Klinische Padiatrie|July 1, 1986
[Guidelines for therapy of idiopathic thrombocytopenic purpura (ITP) in childhood]H Gadner, E R Grümayer, O A Haas
Nature|October 1, 1992
Parental origin of chromosomes involved in the translocation t(9;22)O A Haas, A Argyriou-Tirita, T Lion
Cancer Genetics and Cytogenetics|May 1, 1985
Noninvolvement of chromosome 16 in karyotype evolution of acute myeloid leukemia in a patient with a heritable fragile site on 16q22O A Haas, E Nacheva, J D Schwarzmeier
Cancer|November 1, 1987
Poorly differentiated, neuron-specific enolase positive round cell tumor with two translocations t(11;22) and t(21;22)O A Haas, A Chott, R Ladenstein, et al.
Pageof 21