Craniometaphyseal dysplasia with obvious biochemical abnormality and rickets-like features-Reference-Cited by-同舟云学术

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Craniometaphyseal dysplasia with obvious biochemical abnormality and rickets-like features

Published:2016-05 Issue: Volume:456 Page:122-127
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Wu Bo,Jiang Yan,Wang Ou,Li Mei,Xing Xiao-ping,Xia Wei-bo

Funder

National Natural Science Foundation of China

Beijing Natural Science Foundation

Ministry of Science and Technology of the People's Republic of China

Scientific Research Foundation of Beijing Medical Development

National Key Program of Clinical Science

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference24 articles.

1. Craniometaphyseal dysplasia (CMD), autosomal dominant form;Beighton;J. Med. Genet.,1995

2. Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. III. Progressive diaphyseal dysplasia;Jackson;AMA Arch. Intern. Med.,1954

3. Craniometaphyseal dysplasia: a case report and review of medical and surgical management;Sheppard;Int. J. Pediatr. Otorhinolaryngol.,2003

4. Role of the mouse ank gene in control of tissue calcification and arthritis;Ho;Science,2000

5. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia;Iughetti;Am. J. Med. Genet.,2000

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hypophosphatemic rickets: An unexplained early feature of craniometaphyseal dysplasia;Bone Reports;2023-12

2. Transmastoid Facial Nerve Decompression for Craniometaphyseal Dysplasia;Otology & Neurotology;2023-08-26

3. Three-dimensional radiographic features of craniometaphyseal dysplasia—a comparative CBCT study;Journal of Rare Diseases;2023-04-03

4. A three-year clinical investigation of a Chinese child with craniometaphyseal dysplasia caused by a mutated ANKH gene;World Journal of Clinical Cases;2021-03-16

5. Differences in intracellular localisation of ANKH mutants that relate to mechanisms of calcium pyrophosphate deposition disease and craniometaphyseal dysplasia;Scientific Reports;2020-05-04

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