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A roentgenologic and genetic study of a rare osseous distrophy
Published online by Cambridge University Press: 01 August 2014
Summary
Description is made of a family of which in three generations five members presented a rare osseous distrophy. Medical information was obtained for about 46 individuals of the 107 who constitute the family. The affection shows resemblances with both the Camurati-Engelmann disease and hyperostosis corticalis generalisata familiaris. It is inherited through a dominant gene.
- Type
- Research Article
- Information
- Acta geneticae medicae et gemellologiae: twin research , Volume 10 , Issue 3 , July 1961 , pp. 340 - 352
- Copyright
- Copyright © The International Society for Twin Studies 1961
References
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