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Publicado por Springer, 2009
ISBN 10: 3540763279ISBN 13: 9783540763277
Librería: HPB-Red, Dallas, TX, Estados Unidos de America
Libro
Hardcover. Condición: 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!.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: Phatpocket Limited, Waltham Abbey, HERTS, Reino Unido
Libro
Condición: Good. Your purchase helps support Sri Lankan Children's Charity 'The Rainbow Centre'. Ex-library, so some stamps and wear, but in good overall condition. Our donations to The Rainbow Centre have helped provide an education and a safe haven to hundreds of children who live in appalling conditions.
Publicado por Lippincott Williams & Wilkins,US, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: Aardvark Rare Books, Bucknell, SHROP, Reino Unido
Libro
Hardcover. Condición: New. Shrinkwrapped.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: Books Puddle, New York, NY, Estados Unidos de America
Libro
Condición: Used. pp. xvi + 1564 5th Edition.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: Majestic Books, Hounslow, Reino Unido
Libro
Condición: Used. pp. xvi + 1564 Illus.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: Book Dispensary, Concord, ON, Canada
Libro
Hardcover. Condición: New. 5th or later Edition. BRAND NEW hardcover, sealed in publisher's plastic. Book.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: Jenson Books Inc, Logan, UT, Estados Unidos de America
Libro
hardcover. Condición: Good. This item shows signs of wear from consistent use, but it remains in good condition and works perfectly. All pages and cover are intact , but may have aesthetic issues such as small tears, bends, scratches, and scuffs. Spine may also show signs of wear. Pages may include some notes and highlighting. May include "From the library of" labels. Satisfaction Guaranteed.
Publicado por Williams & Wilkins, 1999
ISBN 10: 0683300555ISBN 13: 9780683300550
Librería: Mispah books, Redhill, SURRE, Reino Unido
Libro
Hardcover. Condición: Like New. Like New. book.
Publicado por Springer, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: booksXpress, Bayonne, NJ, Estados Unidos de America
Libro
Soft Cover. Condición: new.
Publicado por Springer, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: booksXpress, Bayonne, NJ, Estados Unidos de America
Libro
Hardcover. Condición: new.
Publicado por Springer, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: Lucky's Textbooks, Dallas, TX, Estados Unidos de America
Libro
Condición: New.
Publicado por Springer, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: Lucky's Textbooks, Dallas, TX, Estados Unidos de America
Libro
Condición: New.
Publicado por Springer US, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: moluna, Greven, Alemania
Libro
Gebunden. Condición: New.
Publicado por Springer US, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: moluna, Greven, Alemania
Libro
Condición: New.
Publicado por Springer US Jan 1990, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Alemania
Libro Impresión bajo demanda
Buch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Genetic disorders have emerged as a prominent cause of morbidity and mor tality among infants and adults. As many as 10% to 20% of hospital admis sions and at least 10% of the mortality in this age group are due to inherited diseases. There are at least two factors that have brought genetic disorders into the forefront of pediatrics. One is a great reduction in childhood mortality due to infections and nutritional deficiency states, and the other is the rapid progress made in the identification of genetic defects. Amniocentesis, chorionic villus sampling, and recombinant DNA technology have already had a tremendous impact on the practice of medicine. This is why the first two chapters of this volume are dedicated to general principles of molecular genetics and to a description of the techniques used to diagnose genetic disorders at the DNA level. The relevance of this new area of science to the study of inherited renal diseases is reflected in the large body of knowledge that has been generated regarding the association between various glomerular nephritides and genetic markers such as the HLA system, and even more impressively in the direct or indirect identification of abnormal genes or gene products in Alport's syn drome, autosomal dominant polycystic kidney disease, and Lowe's syndrome. These discoveries figure prominently in the pages of this book. Yet, the progress we have made has barely scratched the surface of the problem. 468 pp. Englisch.
Publicado por Springer, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: Ria Christie Collections, Uxbridge, Reino Unido
Libro Impresión bajo demanda
Condición: New. PRINT ON DEMAND Book; New; Fast Shipping from the UK. No. book.
Publicado por Springer, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: Ria Christie Collections, Uxbridge, Reino Unido
Libro Impresión bajo demanda
Condición: New. PRINT ON DEMAND Book; New; Fast Shipping from the UK. No. book.
Publicado por Springer, 2015
ISBN 10: 3662435950ISBN 13: 9783662435953
Librería: SecondSale, Montgomery, IL, Estados Unidos de America
Libro
Condición: Good. Item in good condition. Textbooks may not include supplemental items i.e. CDs, access codes etc.
Publicado por Springer US, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: AHA-BUCH GmbH, Einbeck, Alemania
Libro
Buch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - Genetic disorders have emerged as a prominent cause of morbidity and mor tality among infants and adults. As many as 10% to 20% of hospital admis sions and at least 10% of the mortality in this age group are due to inherited diseases. There are at least two factors that have brought genetic disorders into the forefront of pediatrics. One is a great reduction in childhood mortality due to infections and nutritional deficiency states, and the other is the rapid progress made in the identification of genetic defects. Amniocentesis, chorionic villus sampling, and recombinant DNA technology have already had a tremendous impact on the practice of medicine. This is why the first two chapters of this volume are dedicated to general principles of molecular genetics and to a description of the techniques used to diagnose genetic disorders at the DNA level. The relevance of this new area of science to the study of inherited renal diseases is reflected in the large body of knowledge that has been generated regarding the association between various glomerular nephritides and genetic markers such as the HLA system, and even more impressively in the direct or indirect identification of abnormal genes or gene products in Alport's syn drome, autosomal dominant polycystic kidney disease, and Lowe's syndrome. These discoveries figure prominently in the pages of this book. Yet, the progress we have made has barely scratched the surface of the problem.
Publicado por Springer US, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: AHA-BUCH GmbH, Einbeck, Alemania
Libro
Taschenbuch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - Genetic disorders have emerged as a prominent cause of morbidity and mor tality among infants and adults. As many as 10% to 20% of hospital admis sions and at least 10% of the mortality in this age group are due to inherited diseases. There are at least two factors that have brought genetic disorders into the forefront of pediatrics. One is a great reduction in childhood mortality due to infections and nutritional deficiency states, and the other is the rapid progress made in the identification of genetic defects. Amniocentesis, chorionic villus sampling, and recombinant DNA technology have already had a tremendous impact on the practice of medicine. This is why the first two chapters of this volume are dedicated to general principles of molecular genetics and to a description of the techniques used to diagnose genetic disorders at the DNA level. The relevance of this new area of science to the study of inherited renal diseases is reflected in the large body of knowledge that has been generated regarding the association between various glomerular nephritides and genetic markers such as the HLA system, and even more impressively in the direct or indirect identification of abnormal genes or gene products in Alport's syn drome, autosomal dominant polycystic kidney disease, and Lowe's syndrome. These discoveries figure prominently in the pages of this book. Yet, the progress we have made has barely scratched the surface of the problem.
Publicado por Springer, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: Books Puddle, New York, NY, Estados Unidos de America
Libro
Condición: New. pp. 468.
Publicado por Springer, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: Majestic Books, Hounslow, Reino Unido
Libro Impresión bajo demanda
Condición: New. Print on Demand pp. 468 49:B&W 6.14 x 9.21 in or 234 x 156 mm (Royal 8vo) Perfect Bound on White w/Gloss Lam.
Publicado por Berlin Springer
ISBN 10: 3540763279ISBN 13: 9783540763277
Librería: AHA-BUCH, Einbeck, Alemania
Libro
Gebundene Ausgabe. Condición: Gebraucht. Gebraucht - Sehr gut kompl. 2 Bände, Ungeles.Mängelexpl,Lagerschaden (Knicke/Schmutz, Aufkleber) mögl., Sofortversand - Through 5 editions, Pediatric Nephrology has become the standard reference text for students, trainees, practicing physicians (Pediatricians, Nephrologists, Internists, and Urologists), sub-specialists, and allied health professionals seeking information about Children's Kidney Diseases. It is global in perspective and reflects the international group of editors, who are well-recognized world's experts in Pediatric Nephrology. In a single text, the development of kidney structure and function is followed by detailed and comprehensive chapters on all childhood kidney diseases. These chapters, grouped by major disease categories, utilize molecular and cellular pathophysiology of disease to provide unique and comprehensive information of the current state of the art on all known childhood kidney diseases. Each chapter makes new genetic information easily understandable for the practitioner, and uses many algorithms and diagrams to describe appropriate clinical evaluation of symptoms, differential diagnosis, specific diagnostics, and currently available therapies. The text is not only found in University/Hospital libraries, but on the shelves of sub-specialists, pediatricians, internists, urologists, and extensively in the clinics where it is used during clinical encounters with childhood kidney disease. 2063 pp. Deutsch.
Publicado por Springer US Okt 2011, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Alemania
Libro Impresión bajo demanda
Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Genetic disorders have emerged as a prominent cause of morbidity and mor tality among infants and adults. As many as 10% to 20% of hospital admis sions and at least 10% of the mortality in this age group are due to inherited diseases. There are at least two factors that have brought genetic disorders into the forefront of pediatrics. One is a great reduction in childhood mortality due to infections and nutritional deficiency states, and the other is the rapid progress made in the identification of genetic defects. Amniocentesis, chorionic villus sampling, and recombinant DNA technology have already had a tremendous impact on the practice of medicine. This is why the first two chapters of this volume are dedicated to general principles of molecular genetics and to a description of the techniques used to diagnose genetic disorders at the DNA level. The relevance of this new area of science to the study of inherited renal diseases is reflected in the large body of knowledge that has been generated regarding the association between various glomerular nephritides and genetic markers such as the HLA system, and even more impressively in the direct or indirect identification of abnormal genes or gene products in Alport's syn drome, autosomal dominant polycystic kidney disease, and Lowe's syndrome. These discoveries figure prominently in the pages of this book. Yet, the progress we have made has barely scratched the surface of the problem. 468 pp. Englisch.
Publicado por Springer, 2011
ISBN 10: 1461288878ISBN 13: 9781461288879
Librería: dsmbooks, Liverpool, Reino Unido
Libro
Paperback. Condición: Like New. Like New. book.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: GoldenWavesOfBooks, Fayetteville, TX, Estados Unidos de America
Libro
Hardcover. Condición: new. New. Fast Shipping and good customer service.
Publicado por Springer, 2009
ISBN 10: 3540763279ISBN 13: 9783540763277
Librería: dsmbooks, Liverpool, Reino Unido
Libro
Hardcover. Condición: Like New. Like New. book.
Publicado por Springer, 1990
ISBN 10: 0792302877ISBN 13: 9780792302872
Librería: Mispah books, Redhill, SURRE, Reino Unido
Libro
Hardcover. Condición: Like New. Like New. book.
Publicado por Lippincott Williams & Wilkins, 2003
ISBN 10: 0781735459ISBN 13: 9780781735452
Librería: GoldBooks, Denver, CO, Estados Unidos de America
Libro
Hardcover. Condición: new. New Copy. Customer Service Guaranteed.
Publicado por Springer, 2015
ISBN 10: 3662435950ISBN 13: 9783662435953
Librería: GoldBooks, Denver, CO, Estados Unidos de America
Libro
Hardcover. Condición: new. New Copy. Customer Service Guaranteed.