The Genetics and Development of Scoliosis

Author:   Kenro Kusumi ,  Sally L. Dunwoodie
Publisher:   Springer-Verlag New York Inc.
Edition:   2010 ed.
ISBN:  

9781489982964


Pages:   218
Publication Date:   07 September 2014
Format:   Paperback
Availability:   Manufactured on demand   Availability explained
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The Genetics and Development of Scoliosis


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Overview

Developmental genetic studies of the spine and linkage and family-based association studies have led to recent advances in understanding the genetic etiology of idiopathic, neuromuscular, and congenital forms of scoliosis. The book is written by leaders in genetic and developmental research on scoliosis and developmental studies of the spine.

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Author:   Kenro Kusumi ,  Sally L. Dunwoodie
Publisher:   Springer-Verlag New York Inc.
Imprint:   Springer-Verlag New York Inc.
Edition:   2010 ed.
Dimensions:   Width: 15.50cm , Height: 1.20cm , Length: 23.50cm
Weight:   0.454kg
ISBN:  

9781489982964


ISBN 10:   1489982965
Pages:   218
Publication Date:   07 September 2014
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

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Kenro Kusumi, Ph.D., is an Associate Professor in the School of Life Sciences at Arizona State University and is a founding faculty member at the new University of Arizona College of Medicine-Phoenix in partnership with Arizona State University. Dr. Kusumi’s current research focuses on early spinal development, axial musculoskeletal regeneration, and their applications to genetic studies of scoliosis and other musculoskeletal disorders. Sally L. Dunwoodie, Ph.D., is an Associate Professor at the University of New South Wales and Laboratory Head in the Developmental Biology Division at the Victor Chang Cardiac Research Institute in Sydney. Dr Dunwoodie's research focuses on development of the spine, heart, kidney and placenta in mouse, and their relevance to the molecular basis of congenital abnormalities.

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