Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13
dc.contributor.author | Swaroop, Anand | en_US |
dc.contributor.author | Yang-Feng, Teresa L. | en_US |
dc.contributor.author | Fujita, Ricardo | en_US |
dc.contributor.author | Pakstis, Andrew J. | en_US |
dc.contributor.author | Skolnick, Craig | en_US |
dc.date.accessioned | 2006-09-11T19:13:13Z | |
dc.date.available | 2006-09-11T19:13:13Z | |
dc.date.issued | 1995-04 | en_US |
dc.identifier.citation | Fujita, Ricardo; Skolnick, Craig; Pakstis, Andrew J.; Yang-Feng, Teresa L.; Swaroop, Anand; (1995). "Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13." Human Genetics 95(4): 467-468. <http://hdl.handle.net/2027.42/47638> | en_US |
dc.identifier.issn | 1432-1203 | en_US |
dc.identifier.issn | 0340-6717 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/47638 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7705848&dopt=citation | en_US |
dc.description.abstract | A polymorphic CA repeat (locus name DXS1178 ) was isolated from a 1-megabase YAC (OTCC) containing the OTC gene, located at Xp21.1. However, amplification in human-rodent hybrid cells and segregation analysis in three CEPH families mapped the DXS1178 locus at Xq13. The mapping ambiguity is apparently caused by the chimeric nature of the OTCC YAC clone. | en_US |
dc.format.extent | 109243 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Springer-Verlag | en_US |
dc.subject.other | Human Genetics | en_US |
dc.subject.other | Internal Medicine | en_US |
dc.subject.other | Molecular Medicine | en_US |
dc.subject.other | Metabolic Diseases | en_US |
dc.subject.other | Biomedicine | en_US |
dc.title | Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13 | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbsecondlevel | Genetics | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Ophthalmology, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USA; Department of Human Genetics, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationum | Department of Ophthalmology, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationum | Department of Ophthalmology, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationother | Department of Genetics, Yale University School of Medicine, 06510, New Haven, CT, USA | en_US |
dc.contributor.affiliationother | Department of Genetics, Yale University School of Medicine, 06510, New Haven, CT, USA | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.identifier.pmid | 7705848 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/47638/1/439_2004_Article_BF00208981.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1007/BF00208981 | en_US |
dc.identifier.source | Human Genetics | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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