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International Journal of Oncology|May 17, 2011
Use of fluorescence in-situ hybridization (fish) for the estimation of the aberrant cell clone in leukemias with trisomy-8 or monosomy-7 detected by karyotypingE Gebhart, U Trautmann, S Reichardt, et al.
Acta Biologica Et Medica Germanica|January 1, 1977
[Oxytocinergic exohypothalamic connections to the medulla oblongata in the pigeon and rat]F Schober, U Trautmann, W Naumann, et al.
Annales De Genetique|January 1, 1991
Interstitial deletion of 16(q13q22) in a newborn resulting from a paternal insertional translocationS Edelhoff, B Maier, U Trautmann, et al.
International Journal of Oncology|May 17, 2000
Delimiting the use of comparative genomic hybridization in human myeloid neoplastic disordersE Gebhart, I Verdorfer, W Saul, et al.
Prenatal Diagnosis|April 5, 2001
Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic developmentD Schlembach, M Zenker, U Trautmann, et al.
Anticancer Research|April 13, 2001
The cytogenetic view of standard comparative genomic hybridization (CGH): deletions of 20q in human leukemia as a measure of the sensitivity of the techniqueL Brecevic, I Verdorfer, W Saul, et al.
Cancer Genetics and Cytogenetics|July 1, 1992
Multiple chromosomal changes and karyotypic evolution in a patient with myelofibrosisU Trautmann, A Rubbert, M Gramatzki, et al.
Human Genetics|August 1, 1991
Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probeU Trautmann, G Leuteritz, G Senger, et al.
Human Genetics|July 1, 1995
Familial reciprocal translocation t(17;19) (q11.2;q13.2) associated with neurofibromatosis type 1, including one patient with non-Hodgkin lymphoma and an additional t(14;20) in B lymphocytesR Fahsold, T Habash, U Trautmann, et al.
Annales De Genetique|May 26, 1998
Interstitial deletion del(3)(p12p21) in a malformed child subsequent to paternal paracentric insertion (or intraarm shift) 46,XY, ins(3)(p24.1p12.1p21.31)R A Pfeiffer, A Rauch, R Ulmer, et al.
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