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The new electronic edition of Mitelman's Catalog of Chromosome Aberrations in Cancer continues its legacy as the most complete, up-to-date sourcebook available on the chromosomal changes that have been reported in cases of human neoplastic disorder. Replacing the print version, this CD-ROM is an interactive database which combines all of the information found in the print edition, along with new databases which are currently not included in print. In addition, this electronic version offers all the advantages of searchability and hyperlinked cross references which are unique to this format.
A systematic, concise and uniform presentation of the chromosome changes reported in human neoplastic disorders. Due to the dramatic increase of data, especially on solid tumors which typically have very complex karyotypes, the number of entries has almost doubled in the present edition. This version contains several improvements: all karyotypes have been adjusted according to the ISCN (1991) nomenclature recommendations, extremely complex karyotypes are now displayed unabridged, clonal aberrations are classified by conventional criteria as nonneoplastic disorders/lesions and morphological diagnoses (particularly those of solid tumors) have been reorganized and extended to make retrieval of data on specific tumor types more accessible.
The new electronic edition of Mitelman's Catalog of Chromosome Aberrations in Cancer continues its legacy as the most complete, up-to-date sourcebook available on the chromosomal changes that have been reported in cases of human neoplastic disorder. Replacing the print version, this CD-ROM is an interactive database which combines all of the information found in the print edition, along with new databases which are currently not included in print. In addition, this electronic version offers all the advantages of searchability and hyperlinked cross references which are unique to this format.
A two-volume set, this work is the only complete reference on the subject. It is extensive, systematic and uniform in its presentation and provides clinically important information for the evaluation, diagnosis, treatment and prognosis of neoplastic diseases.
A two-volume set, this work is the only complete reference on the subject. It is extensive, systematic and uniform in its presentation and provides clinically important information for the evaluation, diagnosis, treatment and prognosis of neoplastic diseases.
The first three editions of this acclaimed book presented a much-needed conceptual synthesis of this rapidly moving field. Now, Cancer Cytogenetics, Fourth Edition, offers a comprehensive, expanded, and up-to-date review of recent dramatic advances in this area, incorporating a vast amount of new data from the latest basic and clinical investigations. New contributors reflecting broader international authorship and even greater expertise Greater emphasis throughout on the clinical importance and application of information about cytogenetic and molecular aberrations Includes a complete coverage of chromosome aberrations in cancer based on an assessment of the 60,000 neoplasms cytogenetically investigated to date Now produced in full color for enhanced clarity Covers how molecular genetic data (PCR-based and sequencing information) are collated with the cytogenetic data where pertinent Discusses how molecular cytogenetic data (based on studies using FISH, CGH, SNP, etc) are fused with karyotyping data to enable an as comprehensive understanding of cancer cytogenetics as is currently possible
Researchers involved in the cytogenetics and molecular genetics of human tumors will welcome this comprehensive overview of the type of aberrations that chromosome 12 presents in human solid tumors. The authors study the implications for a cytogenetic subtyping of the tumors involved and strategies for identifying the molecular changes which underlie the karyotypic alterations. The aberrations of chromosome 12 which the book deals with are very frequent chromosomal alterations in human tumors occuring in frequent benign mesenchymal tumors, such as uterine leiomyomas and lipomas, and in tumors of epithelial origin, such as pleomorphic adenomas of the salivary glands.
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