Literature DB >> 1970325

The CEPH consortium primary linkage map of human chromosome 10.

R L White1, J M Lalouel, Y Nakamura, H Donis-Keller, P Green, D W Bowden, C G Mathew, D F Easton, E B Robson, N E Morton.   

Abstract

The first CEPH consortium map, that of chromosome 10, is presented. This primary linkage map contains 28 continuously linked loci defined by genotypes generated from CEPH family DNAs with 37 probe and enzyme combinations. Cytogenetic localization of some of the genetic markers indicates that the consortium map extends, at least, from 10p13 to 10q26. The order of loci on the consortium map agrees with the physical localization data. The female map spans 309 cM (206 cM if an approximation of interference is included in the mapping function used to construct the map), and the mean genetic distance of intervals is 11 cM (7 cM). Also presented are maps of chromosome 10 from each of five CEPH collaborating laboratories, based on genotypes for all relevant markers in the CEPH database. The CEPH consortium map of chromosome 10 should be useful for localization of any gene of interest falling within the span covered. The genotypes in the chromosome 10 consortium map database are now available to the scientific community.

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Year:  1990        PMID: 1970325     DOI: 10.1016/0888-7543(90)90469-b

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Extensive size polymorphism of the human keratin 10 chain resides in the C-terminal V2 subdomain due to variable numbers and sizes of glycine loops.

Authors:  B P Korge; S Q Gan; O W McBride; D Mischke; P M Steinert
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-01       Impact factor: 11.205

2.  The gene for MEN 2A is tightly linked to the centromere of chromosome 10.

Authors:  S A Narod; H Sobol; I Schuffenecker; M F Lavoué; G M Lenoir
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

3.  Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellites.

Authors:  G W Smith; C A Graham; J Nevin; N C Nevin
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

4.  Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10.

Authors:  A E Karlbom; C D James; J Boethius; W K Cavenee; V P Collins; M Nordenskjöld; C Larsson
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

5.  A collection of ordered tetranucleotide-repeat markers from the human genome. The Utah Marker Development Group.

Authors: 
Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025

6.  A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance.

Authors:  H Coon; S Jensen; M Hoff; J Holik; R Plaetke; F Reimherr; P Wender; M Leppert; W Byerley
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

  6 in total

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