FXY2/MID2, a Gene Related to the X-Linked Opitz Syndrome Gene FXY/MID1, Maps to Xq22 and Encodes a FNIII Domain-Containing Protein That Associates with Microtubules
- 15 December 1999
- Vol. 62 (3), 385-394
- https://doi.org/10.1006/geno.1999.6043
Abstract
No abstract availableKeywords
This publication has 51 references indexed in Scilit:
- MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During DevelopmentHuman Molecular Genetics, 1999
- X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between Xq21.33 and Xq23American Journal of Medical Genetics, 1999
- A New Family of Mouse Genes Homologous to the HumanMAGEGenesGenomics, 1999
- RING fingers and B-boxes: zinc-binding protein-protein interaction domainsBiochemistry and Cell Biology, 1998
- Building proteins with fibronectin type III modulesStructure, 1994
- Proposed acquisition of an animal protein domain by bacteria.Proceedings of the National Academy of Sciences, 1992
- cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.Proceedings of the National Academy of Sciences, 1992
- Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genesGenomics, 1990
- Myofibrillar M-band proteins in rat skeletal muscles during developmentHistochemistry and Cell Biology, 1990
- Genetic homology and crossing over in the X and Y chromosomes of mammalsHuman Genetics, 1982