The Genetics of Fibrodysplasia Ossificans Progressiva
- 1 January 1998
- journal article
- research article
- Published by Wolters Kluwer Health
- Vol. 346 (346) , 15???18-18
- https://doi.org/10.1097/00003086-199801000-00004
Abstract
Fibrodysplasia ossificans progressiva is an autosomal dominant disorder. Most cases are due to new gene mutations because people with fibrodysplasia ossificans progressiva have markedly reduced reproductive fitness. The gene or genes responsible for this disorder are unknown.Keywords
This publication has 22 references indexed in Scilit:
- Fibrodysplasia Ossificans Progressiva — Lessons from Rare MaladiesNew England Journal of Medicine, 1996
- Overexpression of an Osteogenic Morphogen in Fibrodysplasia Ossificans ProgressivaNew England Journal of Medicine, 1996
- Fibrodysplasia ossificans progressiva in two half-sisters: Evidence for maternal mosaicismAmerican Journal of Medical Genetics, 1996
- Fine Mapping of the Human Bone Morphogenetic Protein-4 Gene (BMP4) to Chromosome 14q22-q23 by in Situ HybridizationGenomics, 1995
- Myositis Ossificans Progressiva in an African ChildThe British Journal of Radiology, 1966
- Myositis ossificans progressivaThe American Journal of Medicine, 1964
- Early myositis ossificans progressiva occurring in homozygotic twins: A clinical and pathologic studyThe Journal of Pediatrics, 1957
- MYOSITIS OSSIFICANS PROGRESSIVAThe Lancet Healthy Longevity, 1927
- A CONTRIBUTION TO THE STUDY OF MYOSITIS OSSIFICANS PROGRESSIVAAnnals of Surgery, 1918
- MYOSITIS OSSIFICANS.The Lancet, 1892