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Oncology Reports|May 20, 2011
Improved detection of chromosome 16 rearrangements in acute myeloid leukemias using 16p and 16q specific microdissection DNA librariesI Chudoba, N Rubtsov, G Senger, et al.
European Journal of Cancer (Oxford, England : 1990)|November 30, 2000
The homeobox gene MEIS1 is amplified in IMR-32 and highly expressed in other neuroblastoma cell linesT A Jones, R H Flomen, G Senger, et al.
Cytogenetic and Genome Research|May 27, 2004
mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrationsI Chudoba, G Hickmann, T Friedrich, et al.
Cytogenetics and Cell Genetics|July 7, 1999
High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomesI Chudoba, A Plesch, T Lörch, et al.
Cytogenetics and Cell Genetics|February 15, 2001
An SRY-negative 47,XXY mother and daughterS Röttger, K Schiebel, G Senger, et al.
Molecular Endocrinology (Baltimore, Md.)|November 1, 1994
NOT, a human immediate-early response gene closely related to the steroid/thyroid hormone receptor NAK1/TR3H W Mages, O Rilke, R Bravo, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromesK Buiting, S Gross, Y Ji, et al.
Prenatal Diagnosis|April 1, 1997
Prenatal diagnosis of a half-cryptic translocation using chromosome microdissectionG Senger, I Chudoba, U Friedrich, et al.
Human Genetics|July 1, 1989
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndromeH J Lüdecke, R Burdiek, G Senger, et al.
Human Immunology|May 1, 1994
Cloning of the region between HLA-DMB and LMP2 in the human major histocompatibility complexP Sanséau, A Jackson, G Senger, et al.
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