Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
- 1 February 1995
- Vol. 80 (3) , 431-437
- https://doi.org/10.1016/0092-8674(95)90493-x
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesisCell, 1995
- The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mappingCell, 1994
- Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeNature Genetics, 1994
- Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasiaPublished by Elsevier ,1994
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Report of the Second International Workshop on Human Chromosome 6Genomics, 1994
- Type II Collagen Mutations in Rare and CommonAnnals of Medicine, 1994
- A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaNature Genetics, 1993
- Effect of 5' splice site mutations on splicing of the preceding intron.Molecular and Cellular Biology, 1990
- Nucleation, Propagation, and Direction of Triple Helix Formation in Collagens I, III, and IV and in Gelatin as Monitored by Electron MicroscopyaAnnals of the New York Academy of Sciences, 1990