Mutations in CDMP1 cause autosomal dominant brachydactyly type C
- 1 September 1997
- journal article
- other
- Published by Springer Nature in Nature Genetics
- Vol. 17 (1) , 18-19
- https://doi.org/10.1038/ng0997-18
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1Nature Genetics, 1997
- Clinical and locus heterogeneity in brachydactyly type CAmerican Journal of Medical Genetics, 1997
- Brachydactyly Type C Gene Maps to Human Chromosome 12q24Genomics, 1996
- BMP Signaling in Drosophila EmbryogenesisAnnals of the New York Academy of Sciences, 1996
- A human chondrodysplasia due to a mutation in a TGF-β superfamily memberNature Genetics, 1996
- A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye.Genes & Development, 1995
- Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamilyNature, 1994
- The molecular basis of genetic dominance.Journal of Medical Genetics, 1994
- The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamilyCell, 1992
- BRACHYPODISMJournal of Heredity, 1952