A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
- 1 April 1995
- Vol. 81 (1) , 15-25
- https://doi.org/10.1016/0092-8674(95)90367-4
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)Genomics, 1995
- MIC2R: a transcribed MIC2-related sequence associated with a CpG island in the human pseudoautosomal regionHuman Molecular Genetics, 1994
- Isolation of genes from complex sources of mammalian genomic DNA using exon amplificationNature Genetics, 1994
- A high resolution deletion map of human chromosome Xp22Nature Genetics, 1993
- Morquio disease: Isolation, characterization and expression of full-length cDNA for human N-acetylgalactosamine-6-sulfate sulfataseBiochemical and Biophysical Research Communications, 1991
- A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding moleculesNature, 1991
- The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolutionCell, 1988
- Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfataseBiochemical and Biophysical Research Communications, 1988
- Inherited Chondrodysplasia Punctata Due to a Deletion of the Terminal Short Arm of an X ChromosomeNew England Journal of Medicine, 1984
- Chondrodysplasia punctata—23 cases of a mild and relatively common varietyThe Journal of Pediatrics, 1976