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Article
Array-based DNA methylation analysis in classical Hodgkin lymphoma reveals new insights into the mechanisms underlying silencing of B cell-specific genes
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Article
High-throughput experimental verification of predicted tissue-specific and tumor-specific splice isoforms
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Chapter and Conference Paper
From Genes to Proteins: Full Open Reading Frame (ORF) Clones and Their Application in Functional Research
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Chapter and Conference Paper
Handling uncertainty in 3D object recognition using Bayesian networks
In this paper we show how the uncertainty within a 3d recognition process can be modeled using Bayesian nets. Reliable object features in terms of object rims are introduced to allow a robust recognition of in...
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Chapter and Conference Paper
A 3d Object Recognition System with Decision Reasoning under Uncertainty
In this paper we propose a general framework to build a task oriented 3d object recognition system. To cope with noisy data under changing viewing conditions a 3d object recognition system has to acquire senso...
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Chapter and Conference Paper
Sensor Based View Planning Using Vague Scene Representation
In this paper we present an approach for planning the next best sensor action based on the actual knowledge about a scene and based on a given task to be executed. The actual knowledge about the world is model...
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Article
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
X–linked hypophosphatemic rickets (HYP) is a dominant disorder characterised by impaired phosphate uptake in the kidney, which is likely to be caused by abnormal regulation of sodium phosphate cotransport in t...
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Article
Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI)
After the development of efficient methods for the construction of transcription maps of defined genomic regions, the rate-limiting step in the analysis of the coding potentials of these regions is the elucida...
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Article
Fragile X syndrome without CCG amplification has an FMR1 deletion
We describe a patient with typical clinical features of the fragile X syndrome, but without cytogenetic expression of the fragile X or an amplified CCG trinucleotide repeat fragment. The patient has a previous...