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Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneity

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Year: 1986
Type: article
Study design: Observational Study
Source: American Journal of Medical Genetics
DOI: 10.1002/ajmg.1320230309
Authors: D. O. Sillence, K. K. Barlow, W. G. Cole, S. Dietrich, A. P. Garber, D. L. Rimoin, John M. Opitz, James F. Reynolds
Institutions: The University of Sydney, Royal Children's Hospital, Orthopaedic Hospital, Harbor–UCLA Medical Center
Language: English

Topic: Connective tissue disorders research
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: Eunice Kennedy Shriver National Institute of Child Health and Human Development
Award: THE SKELETAL DYSPLASIAS
OpenAlex ID: W2095605099
FWCI: 8.766
Cites: 53
Cited by: 222
Related to: 10
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