Fibrodysplasia Ossificans Progressiva, a Heritable Disorder of Severe Heterotopic Ossification, Maps to Human Chromosome 4q27-31*
- 1 January 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (1) , 128-135
- https://doi.org/10.1086/302724
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Fibrodysplasia (Myositis) Ossificans ProgressivaClinical Orthopaedics and Related Research, 1998
- Overexpression of an Osteogenic Morphogen in Fibrodysplasia Ossificans ProgressivaNew England Journal of Medicine, 1996
- Serine Phosphorylation, Chromosomal Localization, and Transforming Growth Factor-β Signal Transduction by HumanJournal of Biological Chemistry, 1996
- MADR1, a MAD-Related Protein That Functions in BMP2 Signaling PathwaysCell, 1996
- Severe restriction in jaw movement after routine injection of local anesthetic in patients who have fibrodysplasia ossificans progressivaOral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology, 1996
- The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms.Genes & Development, 1994
- A three generation family with fibrodysplasia ossificans progressiva.Journal of Medical Genetics, 1993
- The Transforming Growth Factor-beta FamilyAnnual Review of Cell Biology, 1990
- Novel Regulators of Bone Formation: Molecular Clones and ActivitiesScience, 1988
- Genetic aspects of fibrodysplasia ossificans progressiva.Journal of Medical Genetics, 1982