Idiopathic Hyperphosphatasia andTNFRSF11BMutations: Relationships Between Phenotype and Genotype-Reference-Cited by-同舟云学术

Idiopathic Hyperphosphatasia andTNFRSF11BMutations: Relationships Between Phenotype and Genotype

Published:2003-12 Issue:12 Volume:18 Page:2095-2104
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Chong Belinda,Hegde Madhuri,Fawkner Matthew,Simonet Scott,Cassinelli Hamilton,Coker Mahmut,Kanis John,Seidel Joerg,Tau Cristina,Tüysüz Beyhan,Yüksel Bilgin,Love Donald,Cundy Tim

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference35 articles.

1. Fragile bones and macrocranium;Bakwin;J Pediatr,1956

2. Familial idiopathic hyperphosphatasia;Blanco;J Bone Joint Surg Br,1977

3. Familial hyperphosphatasemia: Diagnosis in early infancy and response to human thyrocalcitonin therapy;Dunn;Am J Roentgenol,1979

4. Hereditary hyperphosphatasia: 20 years follow-up and response to disodium etidronate;Singer;J Bone Miner Res,1994

5. Chronic idiopathic hyperphosphatasia associated with pseudoxanthoma elasticum;Mitsudo;J Bone Joint Surg Am,1971

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