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Titlebook: Integral Equations; Theory and Numerical Wolfgang Hackbusch Book 1995 Birkhäuser Verlag 1995 Approximation.Integral equation.Interpolation

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Wolfgang Hackbuschically in the course of neurofibromatosis 1 (NF1) (usually the plexiform neurofibroma). The deletion in the NF1 gene is responsible for the tumor development in both sporadic and syndromic cases..The lesions are usually in the form of palpable mass and cause no specific symptoms. Diagnostic evaluati
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Wolfgang Hackbuscheurosurgeons, hand surgeons, plastic and orthopedic surgeons new to the field, but also for seasoned specialists who wish to update their knowledge with new insights based on robust experimental and clinical material.  In addition, it will be a helpful tool for general and oncological surgeons who a
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Wolfgang Hackbusch make the coverage especially practical, the book‘s features link the theoretical to the real-world practice of LD assessment, among them:.Overviews of LD identification and definitions..Analysis of widely used diagnostic approaches with strengths and weaknesses..Examples of assessment protocols and
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Wolfgang Hackbusch make the coverage especially practical, the book‘s features link the theoretical to the real-world practice of LD assessment, among them:.Overviews of LD identification and definitions..Analysis of widely used diagnostic approaches with strengths and weaknesses..Examples of assessment protocols and
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Wolfgang Hackbuschn complex clinical samples. Raman spectroscopy is a molecular technique that is capable of probing samples noninvasively and nondestructively. It has been used with high specificity to assess tissue and bacterial samples at the molecular level with diverse clinical and diagnostic applications. SERS
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Wolfgang Hackbuschere detected by capturing chemiluminiscence on instant (e.g., Polaroid) films. Each viable cell (i.e., rRNA producing) is detected as a light spot from its microcolony on the film after scanning the image into a computer. This rapid . hybridization technique is simple and highly sensitive and could
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ence regions of ribosomal DNA or unique bacterial target genes, such as virulence or resistance factors. The microarray is produced using standard spotting equipment with an array layout containing a high number of replicates. Fluorescence scanning of on-chip PCR slides allows the rapid detection of
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