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" The genetics of osteoporosis and metabolic bone disease "
ed. by Michael J. Econs.
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BL
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| Record Number
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726060
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b545790
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| Main Entry
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ed. by Michael J. Econs.
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| Title & Author
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The genetics of osteoporosis and metabolic bone disease\ ed. by Michael J. Econs.
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| Publication Statement
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Totowa, N.J: Humana Press, [2010]
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| Page. NO
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462 Seiten : Illustrationen
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| ISBN
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1617371424
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: 9781617371424
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| Notes
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Originally published in 2000.
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| Contents
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Genetic and Environmental Determinants of Variance in Bone Size, Mass, and Volumetric Density of the Proximal Femur, Ego Seeman. How to Determine If, and by How Much, Genetic Variation Influences Osteoporosis, John L. Hopper. Vitamin D Receptor Gene Polymorphisms and Bone Mineral Homeostasis, Serge Ferrari, Rene Rizzoli, and Jean-Philippe Bonjour. Type 1 Collagen Polymorphisms and Osteoporosis, Stuart H. Ralston. Osteogenesis Imperfecta, Paul A. Dawson and Joan C. Marini. Vitamin D-Dependent Rickets Type I and Type II, Sachiko Kitanaka and Shigeaki Kato. Inherited Phosphate Wasting Disorders, Michael J. Econs and Kenneth E. White. X-Linked Nephrolithiasis/Dent's Disease and Mutations in the ClC-5 Chloride Channel, Steven J. Scheinman and Rajesh V. Thakker. Genetics of Tumoral Calcinosis, Kandaswamy Jayaraj and Kenneth Lyles. Fibrous Dysplasia and the McCune-Albright Syndrome, Lee S. Weinstein. The Molecular Basis for Parathyroid Hormone Resistance in Pseudohypoparathyroidism, Michael A. Levine. Fibrodysplasia Ossificans Progressiva, Eileen M. Shore, John G. Rogers, Roger Smith, Francis H. Gannon, Martin Delatycki, J. Andoni Urtizberea, James Triffitt, Martine Le Merrer, and Frederick S. Kaplan. Disorders Resulting from Inactivating or Activating Mutations in the Ca2+o-Sensing Receptor, Edward M. Brown. Multiple Endocrine Neoplasia Type 1 (MEN1), Rajesh V. Thakker. The Ret Signaling System and Its Role in Hereditary Medullary Thyroid Carcinoma, Robert F. Gagel and Gilbert Cote. Genetics of Paget's Disease of Bone, Frederick R. Singer and Robin J. Leach. Osteopetrosis, L. Lyndon Key, Jr. Hypophosphatasia, Michael P. Whyte. Jansen and Blomstrand: Two Human Chondrodysplasias Caused by PTH/PTHrP Receptor Mutations, Harald Juppner and Caroline Silve. Genetic Linkage Analysis in Human Disease, Suzanne M. Leal and Marcy C. Speer. The Identification of Disease Genes in a Candidate Region, Fiona Francis and Tim M. Strom. Finding Mutations in Disease Genes, Peter S. N. Rowe.Index.
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| Subject
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Bone Diseases, Metabolic -- genetics.
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Genetic Diseases, Inborn.
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Genetic Predisposition to Disease.
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| LC Classification
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RC931.M45E339 2010
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| Added Entry
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Michael J Econs
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