ISBN 10: 9048162963 / ISBN 13: 9789048162963
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Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: The reviewers feel this volume will be an extremely valuable resource for anyone working in a clinical cytogenetics laboratory. The editors are to be congratulated for doing a fine job in compiling this volume.Franks S. Grass, Parke Cytogenetics Laboratory and Hon Fong L. Mark, Brown University Medical School.(The Journal of the Association of Genetic Technologists 30 (3), 2004). Codice inventario libreria

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Riassunto: Critical to the accurate diagnosis of human illness is the need to distinguish clinical features that fall within the normal range from those that do not. That distinction is often challenging and not infrequently requires considerable experience at the bedside. It is not surprising that accurate cytogenetic diagnosis is also often a challenge, especially when chromosome study reveals morphologic findings that raise the question of normality. Given the realization that modern human cytogenetics is just over five decades old, it is noteworthy that thorough documentation of normal chromosome var- tion has not yet been accomplished. One key diagnostic consequence of the inability to distinguish a ?normal? variation in chromosome structure from a pathologic change is a missed or inaccurate diagnosis. Clinical cytogeneticists have not, however, been idle. Rather, progressive biotechnological advances coupled with virtual completion of the human genome project have yielded increasingly better microscopic resolution of chromosome structure. Witness the progress from the early short condensed chromosomes to the later visualization of chromosomes through banding techniques, hi- resolution analysis in prophase, and more recently to analysis by fluorescent in situ hybridization (FISH).

Sinossi: This book is not a panacea. However, it does provide, for the first time in one place, a comprehensive view of human chromosome heteromorphisms, their applications, and their often speculated roles in aberrant chromosome behaviour relating to abnormal phenotype, pregnancy loss and cancer. More significantly, the book is a pictorial atlas for common and unusual heteromorphisms and euchromatic variants as they have been studied both by classical banding techniques and by newer molecular or FISH technologies. To facilitate its use as a laboratory or clinical reference, plates in a pictorial section are organized by chromosome number with the most recent ISCN ideogram, summary and extensive list of references for each chromosome. A final pictorial section is devoted to FISH variants. The book is a work in progress, with submission of new variants encouraged for future editions

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H.E. Wyandt
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ISBN 10: 9048162963 ISBN 13: 9789048162963
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Descrizione libro Springer, 2010. PAP. Condizione libro: New. New Book. Shipped from UK in 4 to 14 days. Established seller since 2000. Codice libro della libreria GB-9789048162963

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Descrizione libro Springer, Netherlands, 2010. Paperback. Condizione libro: New. 1st ed. Softcover of orig. ed. 2004. 229 x 152 mm. Language: English . Brand New Book. Critical to the accurate diagnosis of human illness is the need to distinguish clinical features that fall within the normal range from those that do not. That distinction is often challenging and not infrequently requires considerable experience at the bedside. It is not surprising that accurate cytogenetic diagnosis is also often a challenge, especially when chromosome study reveals morphologic findings that raise the question of normality. Given the realization that modern human cytogenetics is just over five decades old, it is noteworthy that thorough documentation of normal chromosome var- tion has not yet been accomplished. One key diagnostic consequence of the inability to distinguish a normal variation in chromosome structure from a pathologic change is a missed or inaccurate diagnosis. Clinical cytogeneticists have not, however, been idle. Rather, progressive biotechnological advances coupled with virtual completion of the human genome project have yielded increasingly better microscopic resolution of chromosome structure. Witness the progress from the early short condensed chromosomes to the later visualization of chromosomes through banding techniques, hi- resolution analysis in prophase, and more recently to analysis by fluorescent in situ hybridization (FISH). Codice libro della libreria AAZ9789048162963

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Editore: Springer, Netherlands (2010)
ISBN 10: 9048162963 ISBN 13: 9789048162963
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Descrizione libro Springer, Netherlands, 2010. Paperback. Condizione libro: New. 1st ed. Softcover of orig. ed. 2004. 229 x 152 mm. Language: English . Brand New Book. Critical to the accurate diagnosis of human illness is the need to distinguish clinical features that fall within the normal range from those that do not. That distinction is often challenging and not infrequently requires considerable experience at the bedside. It is not surprising that accurate cytogenetic diagnosis is also often a challenge, especially when chromosome study reveals morphologic findings that raise the question of normality. Given the realization that modern human cytogenetics is just over five decades old, it is noteworthy that thorough documentation of normal chromosome var- tion has not yet been accomplished. One key diagnostic consequence of the inability to distinguish a normal variation in chromosome structure from a pathologic change is a missed or inaccurate diagnosis. Clinical cytogeneticists have not, however, been idle. Rather, progressive biotechnological advances coupled with virtual completion of the human genome project have yielded increasingly better microscopic resolution of chromosome structure. Witness the progress from the early short condensed chromosomes to the later visualization of chromosomes through banding techniques, hi- resolution analysis in prophase, and more recently to analysis by fluorescent in situ hybridization (FISH). Codice libro della libreria AAZ9789048162963

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Descrizione libro Condizione libro: New. Bookseller Inventory # ST9048162963. Codice libro della libreria ST9048162963

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H.E. Wyandt, Vijay S. Tonk
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Descrizione libro Springer. Paperback. Condizione libro: new. BRAND NEW, Atlas of Human Chromosome Heteromorphisms (1st ed. Softcover of orig. ed. 2004), H.E. Wyandt, Vijay S. Tonk, Critical to the accurate diagnosis of human illness is the need to distinguish clinical features that fall within the normal range from those that do not. That distinction is often challenging and not infrequently requires considerable experience at the bedside. It is not surprising that accurate cytogenetic diagnosis is also often a challenge, especially when chromosome study reveals morphologic findings that raise the question of normality. Given the realization that modern human cytogenetics is just over five decades old, it is noteworthy that thorough documentation of normal chromosome var- tion has not yet been accomplished. One key diagnostic consequence of the inability to distinguish a "normal" variation in chromosome structure from a pathologic change is a missed or inaccurate diagnosis. Clinical cytogeneticists have not, however, been idle. Rather, progressive biotechnological advances coupled with virtual completion of the human genome project have yielded increasingly better microscopic resolution of chromosome structure. Witness the progress from the early short condensed chromosomes to the later visualization of chromosomes through banding techniques, hi- resolution analysis in prophase, and more recently to analysis by fluorescent in situ hybridization (FISH). Codice libro della libreria B9789048162963

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Descrizione libro Springer, 2009. Condizione libro: New. Editor(s): Wyandt, H.E.; Tonk, Vijay S. Num Pages: 279 pages, biography. BIC Classification: MBGL; MFN; MJW; MMF. Category: (P) Professional & Vocational. Dimension: 240 x 160. Weight in Grams: 456. . 2009. Softcover reprint of hardcover 1st ed. 2004. Paperback. . . . . . Codice libro della libreria V9789048162963

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Descrizione libro Paperback. Condizione libro: New. Not Signed; Critical to the accurate diagnosis of human illness is the need to distinguish clinical features that fall within the normal range from those that do not. That distinction is often challenging and not infrequently requires considerable experience at the bedside. It is not surprising that accurate cy. book. Codice libro della libreria ria9789048162963_rkm

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Descrizione libro Springer. Condizione libro: New. Editor(s): Wyandt, H.E.; Tonk, Vijay S. Num Pages: 279 pages, biography. BIC Classification: MBGL; MFN; MJW; MMF. Category: (P) Professional & Vocational. Dimension: 240 x 160. Weight in Grams: 456. . 2009. Softcover reprint of hardcover 1st ed. 2004. Paperback. . . . . Books ship from the US and Ireland. Codice libro della libreria V9789048162963

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Descrizione libro 2010. Paperback. Condizione libro: New. 1st. 160mm x 240mm x. Paperback. This book is not a panacea. However, it does provide, for the first time in one place, a comprehensive view of human chromosome heteromorphisms, their applications, and their .Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability. 299 pages. 0.456. Codice libro della libreria 9789048162963

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Descrizione libro Springer, 2010. Condizione libro: New. This item is printed on demand for shipment within 3 working days. Codice libro della libreria LP9789048162963

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