Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment-Reference-Cited by-同舟云学术

Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment

Published:2014-04-08 Issue:6 Volume:164 Page:1470-1481
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Van Dijk F.S.¹,Sillence D.O.²

Affiliation:

1. Department of Clinical GeneticsCenter for Connective Tissue DisordersVU University Medical CenterAmsterdamThe Netherlands

2. Discipline of Genetic MedicineThe Children's Hospital at Westmead Clinical SchoolSydney Medical SchoolUniversity of SydneyHead Connective Tissue Dysplasia Management ServiceThe Children's Hospital at WestmeadSydneyAustralia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.36545

Reference69 articles.

1. Intravenous Pamidronate Treatment in Children with Moderate-to-Severe Osteogenesis Imperfecta Started under Three Years of Age

2. Intravenous pamidronate treatment of infants with severe osteogenesis imperfecta

3. The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental development;Bailleul‐Forestier I;EJMG,2008

4. Aspects of the history of Osteogenesis imperfecta (Vrolik's syndrome)

5. Deficiency of Cartilage-Associated Protein in Recessive Lethal Osteogenesis Imperfecta

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