Literature DB >> 3464200

A primary genetic map of chromosome 13q.

M Leppert, W Cavenee, P Callahan, T Holm, P O'Connell, K Thompson, G M Lathrop, J M Lalouel, R White.   

Abstract

We have constructed a primary genetic map spanning most of human chromosome 13. A total of 14 polymorphic DNA sequences and one protein polymorphism provided, after construction of haplotypes, seven markers for the long arm of this chromosome. A panel of cell lines from 30 three-generation families with large sibship size served as the sample set. Pairwise cross analysis of the inheritance patterns of the marker loci established that six of the seven loci constituted a single linkage group; the seventh was localized by physical means. Significantly higher recombination rates were found in female than in male meioses in several intervals. The six closely linked loci were arranged, based on the two-point data, in three clusters, and a number of alternate gene orders were excluded by three-point linkage tests. The order and spacing of the individual loci were refined by linkage analyses that considered five loci jointly.

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Year:  1986        PMID: 3464200      PMCID: PMC1683981     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  15 in total

1.  Sex differences in recombination of linked genes in animals.

Authors:  L C Dunn; D Bennett
Journal:  Genet Res       Date:  1967-04       Impact factor: 1.588

2.  Unusual recombination values and the mapping of the lethal miniature in the house mouse.

Authors:  M E Wallace; S A Mallyon
Journal:  Genet Res       Date:  1972-12       Impact factor: 1.588

3.  Esterase D: a new human polymorphism.

Authors:  D A Hopkinson; M A Mestriner; J Cortner; H Harris
Journal:  Ann Hum Genet       Date:  1973-10       Impact factor: 1.670

4.  Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Authors:  W K Cavenee; T P Dryja; R A Phillips; W F Benedict; R Godbout; B L Gallie; A L Murphree; L C Strong; R L White
Journal:  Nature       Date:  1983 Oct 27-Nov 2       Impact factor: 49.962

5.  Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

Authors:  W Cavenee; R Leach; T Mohandas; P Pearson; R White
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

6.  Information gain in joint linkage analysis.

Authors:  E A Thompson
Journal:  IMA J Math Appl Med Biol       Date:  1984

7.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

8.  Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14.

Authors:  R S Sparkes; M C Sparkes; M G Wilson; J W Towner; W Benedict; A L Murphree; J J Yunis
Journal:  Science       Date:  1980-05-30       Impact factor: 47.728

9.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

Review 10.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

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  26 in total

1.  A new, low frequency MspI allele at the D13S3 locus.

Authors:  A Chidambaram; L C Strong; R E Ferrell
Journal:  Nucleic Acids Res       Date:  1990-03-11       Impact factor: 16.971

2.  RFLP in human F13A gene.

Authors:  P Jagadeeswaran
Journal:  Nucleic Acids Res       Date:  1990-03-11       Impact factor: 16.971

3.  Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease.

Authors:  J Schleutker; L Haataja; M Renlund; L Puhakka; J Viitala; L Peltonen; P Aula
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

4.  Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.

Authors:  A Figus; R Lampis; M Devoto; M S Ristaldi; A Ideo; S de Virgilis; A M Nurchi; A Corrias; R Corda; M E Lai
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

5.  Efficient computations in multilocus linkage analysis.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

6.  Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.

Authors:  L A Farrer; B Bonne-Tamir; M Frydman; A Magazanik; K K Kidd; A M Bowcock; L L Cavalli-Sforza
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

7.  Loss of heterozygosity and K-ras gene mutations in gastric cancer.

Authors:  G N Ranzani; B Renault; N S Pellegata; P Fattorini; E Magni; F Bacci; D Amadori
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

8.  Mapping approaches to gene identification in humans.

Authors:  R L White; J M Lalouel; G M Lathrop; M F Leppert; Y Nakamura; P O'Connell
Journal:  West J Med       Date:  1987-10

9.  Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

Authors:  A M Bowcock; L A Farrer; L L Cavalli-Sforza; J M Hebert; K K Kidd; M Frydman; B Bonne-Tamir
Journal:  Am J Hum Genet       Date:  1987-07       Impact factor: 11.025

10.  Eight closely linked loci place the Wilson disease locus within 13q14-q21.

Authors:  A M Bowcock; L A Farrer; J M Hebert; M Agger; I Sternlieb; I H Scheinberg; C H Buys; H Scheffer; M Frydman; T Chajek-Saul
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

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