The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
The type II collagenopathies: A spectrum of chondrodysplasias
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Citations
Cites
Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects
(2002) · Wiley eBooks · doi:10.1002/0471221929 · Cited by 949
Heritable Diseases of Collagen
Prockop, D. J., & Kivirikko, K. I. (1984) · New England Journal of Medicine · doi:10.1056/nejm198408093110606 · Cited by 566
Mutations in collagen genes: causes of rare and some common diseases in humans
Kuivaniemi, H., Tromp, G., & Prockop, D. J. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.7.2010058 · Cited by 479
Hereditary Progressive Arthro-Ophthalmopathy
(2018) · Encyclopedia of Ophthalmology · doi:10.1007/978-3-540-69000-9_100776 · Cited by 476
Holder, S. E. (1991) · Archives of Disease in Childhood · doi:10.1136/adc.66.8.1005 · Cited by 424
Ahmad, N. N., Ala-Kokko, L., Knowlton, R. G., Jimenez, S. A., Weaver, E. J., Maguire, J. I., Tasman, W., & Prockop, D. J. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.15.6624 · Cited by 316
Ala-Kokko, L., Baldwin, C. T., Moskowitz, R. W., & Prockop, D. J. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.17.6565 · Cited by 279
A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
Warman, M. L., Abbott, M., Apte, S. S., Hefferon, T., McIntosh, I., Cohn, D. H., Hecht, J. T., Olsen, B. R., & Francomano, C. A. (1993) · Nature Genetics · doi:10.1038/ng0993-79 · Cited by 261
Identification of the Molecular Defect in a Family with Spondyloepiphyseal Dysplasia
Lee, B., Vissing, H., Ramirez, F., Rogers, D., & Rimoin, D. (1989) · Science · doi:10.1126/science.2543071 · Cited by 244
Jacenko, O., LuValle, P. A., & Olsen, B. R. (1993) · Nature · doi:10.1038/365056a0 · Cited by 211
Cited by
Clinical and molecular genetics of Stickler syndrome
Snead, M. P., & Yates, J. R. W. (1999) · Journal of Medical Genetics · doi:10.1136/jmg.36.5.353 · Cited by 448
Metadata
- Authors
- Spranger, J., Winterpacht, A., & Zabel, B.
- Venue
- European Journal of Pediatrics
- Published
- 1994-02
- Volume
- 153
- Issue
- 2
- Pages
- 56-65
- ISSN
- 0340-6199 (ISSN-L)
- 1432-1076
- OpenAlex
- W2031665650
- Cited by
- 261
- References
- 40
- FWCI
- 8.58
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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How to cite
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- This page
- CoChat. (2026). Citation check: The type II collagenopathies: A spectrum of chondrodysplasias. https://app.cochat.ai/papers/10.1007/bf01959208
- The paper
- Spranger, J., Winterpacht, A., & Zabel, B. (1994). The type II collagenopathies: A spectrum of chondrodysplasias. European Journal of Pediatrics. https://doi.org/10.1007/bf01959208
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
