OHIO ENCYCLOPEDIA is the definitive reference work on Ohio ever published. The noted Ohio historian Michael S. Mangus from Ohio State University has written articles on Introduction to Ohio History, Early History of Ohio, and Ohio History. These articles cover the history of Ohio, from the early explorers to twenty-first century events. Other major sections in this reference work are Ohio Symbols and Designations, Geography and Topography of Ohio, Profiles of Ohio Governors, Chronology of Ohio Historic Events, Dictionary of Ohio Places, Ohio Constitution, Bibliography of Ohio Books, Pictorial Scenes of Ohio, State Executive Offices, State Agencies, Departments and Offices, Ohio Senators, Ohio Assembly Members, U.S. Senators and U.S. Congress members from Ohio, Directory of Ohio Historic Places and Index. All sections contain the latest up to date information on the Buckeye State.OHIO ENCYCLOPEDIA contains stunning photographs and portraits to compliment the expertly written text. Population charts are arranged alphabetically by city or town name, and by county. This allows students easy access to find population figures for their area of interest. Other population charts list all places in Ohio by largest populated places to least populated places by city or county. Several directories contain information on elected state and federal officials along with their contact information including mail and email addresses, phone and fax numbers. Easy to use reference maps are included to find your newly elected state or federal officials. The Directory of State Services lists the head officials and full contact information on state agencies and departments, some of which were just newly created by the legislature. The Directory of Ohio Historic Places contains all the latest up to date information on every Ohio historic place. The Bibliography includes that latest books published on Ohio people and places. A detailed Index makes the work thoroughly referential. OHIO ENCYCLCOPEDIA offers librarians, teachers and students a single source reference work that provides the answers to the most frequently asked questions about Ohio and its history.
Human Chromosome Variation: Heteromorphism and Polymorphism was formerly printed under the title “Atlas of Human Chromosome Heteromorphism”. The Atlas has become a standard reference book in most cytogenetic laboratories and is cited as a significant reference in ISCN 2009. This revised version has updated and retained the most useful pictorial sections of the first edition, including the comprehensive review of normal and “not-so-normal” variations of the human karyotype with summaries and extensive reference lists organized by chromosome number. This updated edition features concise background information on chromosome methods and applications, essential information on heteromorphism frequencies in normal and clinical populations as well as new listing and discussions of euchromatic, subtelomeric and FISH variants. The addition of two new sections make this an even more valuable reference than before. A section on common and rare fragile sites includes a short historical discussion, definitions and an extensive table of officially recognized sites that includes the HUGO name, chromosomal location, methods of induction, genes and references to the most recent molecular characterization. A new section on array CGH discusses the clinical challenge of interpreting copy number variations (CNVs) revealed by this newest technology, gives examples of various levels of interpretation and lists the several most common websites used in this interpretation.
This new edition now titled “Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis” provides the reader with an up-to-date overview of microarrays, fragile sites, copy number variations and whole genome sequencing. Greatly expanding the discussion of microarray analysis in the previous edition of the book, are new chapters on microarray and genomic analysis, plus comprehensive tables on the subtle microdeletions and microduplications that are found on each chromosome, including 235 recurring copy number variants that are associated with well-established or emerging chromosomal syndromes. The current edition features concise information on cytogenetic methods and applications, extending these discussions to DNA analysis and genome sequencing. Sections on euchromatin, heterochromatin, FISH pattern, fragile site, copy number, and DNA sequence variation are integrated with actual clinical examples from cytogenetic laboratories and from clinical practice. The principles that allow for the distinction between benign chromosome / DNA variation and pathogenic heteromorphisms / polymorphisms are discussed and include references to the latest organizational guidelines and genomic or population databases. The two previous incarnations of this book: the ‘Atlas of Human Chromosome Heteromorphism’, and ‘Human Chromosome Variation: Heteromorphism and Polymorphism’ have been standard reference works in most cytogenetic laboratories, used by laboratory directors and clinicians all around the world. While widely used sections from the previous edition on cytogenetic technologies and heteromorphisms are retained intact the present volume adds extensive material on copy number variations (polymorphisms detected by microarray analysis), fragile sites in disease and cancer, and practical views on interpreting emerging technologies, including whole exome sequencing. This book should be of interest to clinicians, technicians and students who are or will be exposed to DNA and/or chromosome analysis and the data derived from these continuously developing techniques. This fully updated book volume will bring the reader up to speed on the latest technologies, their applications, benefits and drawbacks and as such, is a must read for anyone with an interest in DNA and chromosome analysis and the distinction between benign variation and pathogenic mistakes.
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