Genetic Mapping of the Camurati-Engelmann Disease Locus to Chromosome 19q13.1-q13.3
- 1 January 2000
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 66 (1), 143-147
- https://doi.org/10.1086/302728
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
This publication has 25 references indexed in Scilit:
- Decreased bone mass and bone elasticity in mice lacking the transforming growth factor-β1 geneBone, 1998
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Avoiding Recomputation in Linkage AnalysisHuman Heredity, 1994
- Localization of the Human Bona Fide Calmodulin Genes CALM1, CALM2, and CALM3 to Chromosomes 14q24-q31, 2p21.1-p21.3, and 19q13.2-q13.3Genomics, 1993
- Localization of the expression of types I, III, and IV collagen, TGF-β1 and c-fos genes in developing human calvarial bonesDevelopmental Biology, 1988
- Transforming growth factor β gene maps to human chromosome 19 long arm and to mouse chromosome 7Somatic Cell and Molecular Genetics, 1986
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984
- Engelmann's disease of bone--a systemic disorder?Annals Of The Rheumatic Diseases, 1982
- Muscular changes in Engelmann's disease.Archives of Disease in Childhood, 1980
- Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature.Journal of Medical Genetics, 1972