Literature DB >> 1981049

A refined linkage map for DNA markers around the pericentromeric region of chromosome 10.

J S Wu1, S Myers, N Carson, J R Kidd, L Anderson, C M Castiglione, L S Hoyle, J B Lichter, V P Sukhatme, N E Simpson.   

Abstract

A refined genetic linkage map for the pericentromeric region of human chromosome 10 has been constructed from data on 12 distinct polymorphic DNA loci as well as the locus for multiple endocrine neoplasia type 2A (MEN 2A), a dominantly inherited cancer syndrome. The map extends from D10S24 (at 10p13-p12.2) to D10S3 (at 10q21-q23) and is about 70 cM long. Overall, higher female than male recombination frequencies were observed for this region, with the most remarkable female excess in the immediate vicinity of the centromere, as previously reported. Most of the DNA markers in this map are highly informative for linkage and the majority of the interlocus intervals are no more than 6 cM apart. Thus this map should provide a fine framework for future efforts in more detailed mapping studies around the centromeric area. A set of ordered cross-overs identified in this work is a valuable resource for rapidly and accurately localizing new DNA clones isolated from the pericentromeric region.

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Year:  1990        PMID: 1981049     DOI: 10.1016/0888-7543(90)90032-p

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


  6 in total

1.  Status of the search for a major genetic locus for affective disorder in the Old Order Amish.

Authors:  A J Pakstis; J R Kidd; C M Castiglione; K K Kidd
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

2.  Construction of radiation-reduced hybrids and their use in mapping of microclones from chromosome 10p11.2-q11.2.

Authors:  S Fujita; E Shin; T Nakamura; H Kurahashi; Y Kaneda; K Tanaka; T Mori; S Takai; I Nishisho
Journal:  Jpn J Hum Genet       Date:  1993-12

3.  Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.

Authors:  S A Narod; M F Lavoué; K Morgan; C Calmettes; H Sobol; P J Goodfellow; G M Lenoir
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

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.  Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs.

Authors:  J R Howe; T C Lairmore; S K Mishra; S Dou; R Veile; S A Wells; H Donis-Keller
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

Review 6.  Traces of embryogenesis are the same in monozygotic and dizygotic twins: not compatible with double ovulation.

Authors:  Charles E Boklage
Journal:  Hum Reprod       Date:  2009-02-27       Impact factor: 6.918

  6 in total

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