Genetic linkage of mild pseudoachondroplasia (PSACH) to markersin the pericentromeric region of chromosome 19
- 31 December 1993
- Vol. 18 (3) , 656-660
- https://doi.org/10.1016/s0888-7543(05)80369-6
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Linkage of typical pseudoachondroplasia to chromosome 19Genomics, 1993
- Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) geneHuman Molecular Genetics, 1993
- A Mutation in the Amino-Terminal End of the Triple Helix of Type II Collagen Causing Severe OsteochondrodysplasiaGenomics, 1993
- Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysisNature Genetics, 1993
- Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectNature Genetics, 1993
- Multiple epiphyseal dysplasia, Fairbank type: Morphologic and biochemical study of cartilageAmerican Journal of Medical Genetics, 1993
- Exclusion of type II and type VI procollagen gene mutations in a five‐generation family with multiple epiphyseal dysplasiaAmerican Journal of Medical Genetics, 1993
- Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasiaAmerican Journal of Medical Genetics, 1992
- A Comprehensive Genetic Linkage Map of the Human GenomeScience, 1992
- International classification of osteochondrodysplasiasAmerican Journal of Medical Genetics, 1992