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Books > Medicine > Clinical & internal medicine > Musculoskeletal medicine

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Molecular Genetics of Pediatric Orthopaedic Disorders (Hardcover, 2015 ed.) Loot Price: R3,703
Discovery Miles 37 030
Molecular Genetics of Pediatric Orthopaedic Disorders (Hardcover, 2015 ed.): Carol A. Wise, Jonathan J. Rios

Molecular Genetics of Pediatric Orthopaedic Disorders (Hardcover, 2015 ed.)

Carol A. Wise, Jonathan J. Rios

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Loot Price R3,703 Discovery Miles 37 030 | Repayment Terms: R347 pm x 12*

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In the past two decades we have seen a surge forward in understanding the genetics and biochemistry underlying many pediatric orthopaedic disorders. A few projects have even progressed into the realm of clinical trials that are primarily aimed at controlling progressive disease. Meanwhile, genomic technology development has outpaced expectations and is enabling gene discovery for disorders that were previously intractable with traditional genetic methods. Included in this latter category are common disorders that display multigenic inheritance, sporadic disorders, and very rare conditions that are difficult to ascertain. Simultaneously, the study of pediatric orthopaedic disorders has been continuously refined and updated, highlighting a number of likely genetic conditions that are as yet unsolved. Molecular Genetics of Pediatric Orthopaedic Disorders updates researchers and clinicians of new developments of pediatric orthopaedic genetics. The chapters inform the audience on the revolution in new genomic methods and the impact this is having on potential study designs and the potential to discover genetic causes of many unsolved orthopaedic conditions. Recent examples have been included of pediatric orthopaedic conditions, both rare and common, that are being solved with these new methods. The book also educates pediatric orthopedic clinicians and geneticists on our understanding of the biology of "classic" genetic diseases that were derived from prior genetic studies. Chapters include biobanks and strategies for studying very rare disorders, genes and pathways causing primordial dwarfism, and notch signaling in congenital scoliosis, and more.

General

Imprint: Springer-Verlag New York
Country of origin: United States
Release date: March 2015
First published: 2015
Editors: Carol A. Wise • Jonathan J. Rios
Dimensions: 235 x 155 x 11mm (L x W x T)
Format: Hardcover
Pages: 168
Edition: 2015 ed.
ISBN-13: 978-1-4939-2168-3
Categories: Books > Medicine > Pre-clinical medicine: basic sciences > Medical genetics
Books > Medicine > Clinical & internal medicine > Musculoskeletal medicine
Books > Medicine > Surgery > Orthopaedics & fractures
Books > Medicine > General issues > Medical equipment & techniques > Medical research
Books > Medicine > Clinical & internal medicine > Paediatric medicine > General
LSN: 1-4939-2168-1
Barcode: 9781493921683

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