Natural variation in four human collagen genes across an ethnically diverse population
- 30 April 2008
- Vol. 91 (4) , 307-314
- https://doi.org/10.1016/j.ygeno.2007.12.008
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaNature Genetics, 2007
- A "Silent" Polymorphism in the MDR 1 Gene Changes Substrate SpecificityScience, 2007
- Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansHuman Mutation, 2007
- Statistical Tests for Detecting Positive Selection by Utilizing High-Frequency VariantsGenetics, 2006
- CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis ImperfectaCell, 2006
- Sequencing errors or SNPs at splice-acceptor guanines in dbSNP?Nature Biotechnology, 2006
- An initial map of insertion and deletion (INDEL) variation in the human genomeGenome Research, 2006
- Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptorHuman Molecular Genetics, 2003
- The Human Genome Browser at UCSCGenome Research, 2002
- Construction of Phylogenetic TreesScience, 1967