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paperback. Condition: Very Good. Fast Shipping - Safe and Secure 7 days a week!
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Inherited Cardiac Disease (Oxford Specialist Handbooks in Cardiology)
Language: English
Published by Oxford University Press, 2011
ISBN 10: 0199559686 ISBN 13: 9780199559688
Flexibound. Condition: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority!
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Inherited Cardiac Disease
Language: English
Published by Oxford University Press, Incorporated, 2011
ISBN 10: 0199559686 ISBN 13: 9780199559688
Seller: Better World Books Ltd, Dunfermline, United Kingdom
Seller rating 5 out of 5 stars
Condition: Good. Former library copy. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Includes library markings. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.
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Condition: Fair. This is an ex-library book and may have the usual library/used-book markings inside.This book has soft covers. In fair condition, suitable as a study copy. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,300grams, ISBN:9780199559688.
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Condition: New.
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Condition: As New. Unread book in perfect condition.
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Genomics and Health in the Developing World (Oxford Monographs on Medical Genetics)
Book 11 of 21: Oxford Monographs on Medical GeneticsLanguage: English
Published by Oxford University Press, 2012
ISBN 10: 0195374754 ISBN 13: 9780195374759
Seller: ChristianBookbag / Beans Books, Inc., Westlake, OH, U.S.A.
Seller rating 5 out of 5 stars
Hardcover. Condition: Very Good. Scratch and dent. Cover may have wear, dings, tears, other damage, or be missing dust jacket. Buy multiples from our store to save on shipping.
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Clinical and Molecular Heterogeneity of Osteogenesis Imperfecta
Language: English
Published by Morgan and Claypool Publishers, US, 2017
ISBN 10: 1615047441 ISBN 13: 9781615047444
Paperback. Condition: New. Osteogenesis imperfecta (OI) is a disease encompassing a group of disorders mainly characterized by bone fragility and is the commonest form of heritable bone fragility. In this book, the clinical presentations with particular emphasis on rare phenotypes associated with OI are discussed together with molecular advances in diagnosis and treatment of OI. There is a broad spectrum of clinical severity in OI, ranging from multiple fractures in utero and perinatal death, to near-normal adult stature and low fracture incidence. Facial dysmorphism has been noted, but is not well described, nor is it an invariable feature. Sillence et al., in 1979, provided the clinical classification, which has been further expanded. Genetic defects in type 1 collagen can be identified in 85% of patients with a clinical diagnosis of OI, that is, mutations in COL1A1/COL1A2, which follows an autosomal dominant pattern of inheritance. Several genes have now been implicated in autosomal recessive forms of OI and X-linked osteoporosis. Given the possible antenatal presentation and prognosis associated with OI, it is important to make this diagnosis early and be able to distinguish this from other lethal skeletal dysplasias. It is also important to distinguish nonaccidental injury from a pathological cause of fractures, such as OI, and diagnose this promptly in these situations. However, this is not always possible due to variability in presentation and inability to pinpoint the precise genetic etiology despite extensive genetic testing. OI is one such rare genetic condition where treatment is available in the form of bisphosphonates, which has a huge impact on quality of life. Despite advances in medical therapy, multidisciplinary management including physiotherapy remains the mainstay of treatment and improved outcomes in OI.
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Clinical and Molecular Heterogeneity of Osteogenesis Imperfecta
Language: English
Published by Morgan and Claypool Publishers, US, 2017
ISBN 10: 1615047441 ISBN 13: 9781615047444
Seller: Rarewaves.com USA, London, LONDO, United Kingdom
Seller rating 5 out of 5 stars
Paperback. Condition: New. Osteogenesis imperfecta (OI) is a disease encompassing a group of disorders mainly characterized by bone fragility and is the commonest form of heritable bone fragility. In this book, the clinical presentations with particular emphasis on rare phenotypes associated with OI are discussed together with molecular advances in diagnosis and treatment of OI. There is a broad spectrum of clinical severity in OI, ranging from multiple fractures in utero and perinatal death, to near-normal adult stature and low fracture incidence. Facial dysmorphism has been noted, but is not well described, nor is it an invariable feature. Sillence et al., in 1979, provided the clinical classification, which has been further expanded. Genetic defects in type 1 collagen can be identified in 85% of patients with a clinical diagnosis of OI, that is, mutations in COL1A1/COL1A2, which follows an autosomal dominant pattern of inheritance. Several genes have now been implicated in autosomal recessive forms of OI and X-linked osteoporosis. Given the possible antenatal presentation and prognosis associated with OI, it is important to make this diagnosis early and be able to distinguish this from other lethal skeletal dysplasias. It is also important to distinguish nonaccidental injury from a pathological cause of fractures, such as OI, and diagnose this promptly in these situations. However, this is not always possible due to variability in presentation and inability to pinpoint the precise genetic etiology despite extensive genetic testing. OI is one such rare genetic condition where treatment is available in the form of bisphosphonates, which has a huge impact on quality of life. Despite advances in medical therapy, multidisciplinary management including physiotherapy remains the mainstay of treatment and improved outcomes in OI.
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Molecular Biology of Chronic Heart Failure
Language: English
Published by Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045562 ISBN 13: 9781615045563
Condition: New.
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Genomics and Society: Ethical, Legal, Cultural and Socioeconomic Implications
Language: English
Published by Academic Press (edition 1), 2015
ISBN 10: 0124201954 ISBN 13: 9780124201958
Hardcover. Condition: Very Good. 1. It's a well-cared-for item that has seen limited use. The item may show minor signs of wear. All the text is legible, with all pages included. It may have slight markings and/or highlighting.
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The Molecular Biology of Chronic Heart Failure (Paperback or Softback)
Language: English
Published by Morgan & Claypool 2/1/2013, 2013
ISBN 10: 1615045562 ISBN 13: 9781615045563
Paperback or Softback. Condition: New. The Molecular Biology of Chronic Heart Failure. Book.
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paperback. Condition: Fine. Open Books is a nonprofit social venture that provides literacy experiences for thousands of readers each year through inspiring programs and creative capitalization of books.
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Genomic Medicine Skills and Competencies (Genomic and Precision Medicine in Clinical Practice)
Seller: World of Books (was SecondSale), Montgomery, IL, U.S.A.
Seller rating 5 out of 5 stars
Condition: Good. Item in good condition. Textbooks may not include supplemental items i.e. CDs, access codes etc.
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Genomic Medicine Skills and Competencies (Genomic and Precision Medicine in Clinical Practice)
Seller: World of Books (was SecondSale), Montgomery, IL, U.S.A.
Seller rating 5 out of 5 stars
Condition: Very Good. Item in very good condition! Textbooks may not include supplemental items i.e. CDs, access codes etc.
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Flexibound. Condition: Used; Very Good. ***Simply Brit*** Welcome to our online used book store, where affordability meets great quality. Dive into a world of captivating reads without breaking the bank. We take pride in offering a wide selection of used books, from classics to hidden gems, ensuring there is something for every literary palate. All orders are shipped within 24 hours and our lightning fast-delivery within 48 hours coupled with our prompt customer service ensures a smooth journey from ordering to delivery. Discover the joy of reading with us, your trusted source for affordable books that do not compromise on quality.
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Molecular Biology of Chronic Heart Failure
Language: English
Published by Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045562 ISBN 13: 9781615045563
Condition: As New. Unread book in perfect condition.
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Clinical and Molecular Heterogeneity of Osteogenesis Imperfecta (Colloquium Genomic and Molecular Medicine)
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 31.48
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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Clinical and Molecular Heterogeneity of Osteogenesis Imperfecta
Language: English
Published by Morgan & Claypool Life Sciences 2017-01, 2017
ISBN 10: 1615047441 ISBN 13: 9781615047444
PF. Condition: New.
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Paperback. Condition: Brand New. 1st edition. 63 pages. 9.00x7.25x0.25 inches. In Stock.
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Clinical and Molecular Heterogeneity of Osteogenesis Imperfecta
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: New.
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Clinical and Molecular Heterogeneity of Osteogenesis Imperfecta
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: As New. Unread book in perfect condition.
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INHERITED CARDIAC DISEASE
Language: English
Published by Oxford University Press, 2011
ISBN 10: 0199559686 ISBN 13: 9780199559688
Condition: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
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The Molecular Biology of Chronic Heart Failure (Colloquium Series on Genomic and Molecular Medicine, 3)
Language: English
Published by Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045562 ISBN 13: 9781615045563
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 40.89
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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The Molecular Biology of Chronic Heart Failure (Colloquium Series on Genomic and Molecular Medicine)
Language: English
Published by Morgan & Claypool Life Sciences 2013-03-12, 2013
ISBN 10: 1615045562 ISBN 13: 9781615045563
Paperback. Condition: New.
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Condition: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
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Molecular Biology of Chronic Heart Failure
Language: English
Published by Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045562 ISBN 13: 9781615045563
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: New.
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Genomics and Society: Ethical,
Seller: World of Books (was SecondSale), Montgomery, IL, U.S.A.
Seller rating 5 out of 5 stars
Condition: Very Good. Item in very good condition! Textbooks may not include supplemental items i.e. CDs, access codes etc.
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Paperback. Condition: Brand New. 80 pages. 9.25x7.50x0.25 inches. In Stock.
