Literature DB >> 8188250

CEPH consortium Map of chromosome 9.

J Attwood1, M Chiano, A Collins, H Donis-Keller, N Dracopoli, J Fountain, C Falk, D Goudie, J Gusella, J Haines.   

Abstract

This paper describes the Centre d'Etude du Polymorphisme Humain (CEPH) consortium linkage map of chromosome 9. A total of 124 markers were typed in the CEPH family DNAs by 14 contributing laboratories; of these, 42 loci are ordered on the map with likelihood support of at least 1000:1. The uniquely placed markers include 31 that can be typed by PCR. A further 28 markers that can be typed by PCR are approximately positioned on the map. Multilocus linkage analysis with CRI-MAP has produced male, female, and sex-averaged maps extending for 176, 237, and 209 cM, respectively, while sex-averaged maps produced with MAPMAKER and the multiple two-point program MAP extended for 170 and 129 cM, respectively. The male map contains only two intervals greater than 10 cM, and the mean genetic distance between the 42 uniquely placed loci is 4.3 cM. However, no markers were available to anchor the map at either telomere or the centromere. The results confirm the high level of interference suggested by chiasma maps of chromosome 9. Detailed meiotic breakpoints for three of the families are shown. These can be used to provide rapid placement of any new marker without the need for statistical analysis.

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Year:  1994        PMID: 8188250     DOI: 10.1006/geno.1994.1049

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


  6 in total

1.  Characterization of human crossover interference.

Authors:  K W Broman; J L Weber
Journal:  Am J Hum Genet       Date:  2000-05-08       Impact factor: 11.025

2.  Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

Authors:  G M Brown; M Leversha; M Hulten; M A Ferguson-Smith; N A Affara; R A Furlong
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

3.  A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels.

Authors:  S C Gerken; H Albertsen; T Elsner; L Ballard; P Holik; E Lawrence; M Moore; X Zhao; R White
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

4.  Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.

Authors:  T Toda; S Ikegawa; K Okui; E Kondo; K Saito; Y Fukuyama; M Yoshioka; T Kumagai; K Suzumori; I Kanazawa
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

5.  A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.

Authors:  M Bamshad; W S Watkins; R K Zenger; J F Bohnsack; J C Carey; B Otterud; P A Krakowiak; M Robertson; L B Jorde
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

6.  Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group.

Authors:  M Krajinovic; B Pinamonti; G Sinagra; M Vatta; G M Severini; J Milasin; A Falaschi; F Camerini; M Giacca; L Mestroni
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

  6 in total

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