Literature DB >> 3243552

Twelve loci form a continuous linkage map for human chromosome 18.

P O'Connell1, G M Lathrop, M Leppert, Y Nakamura, U Müller, J M Lalouel, R White.   

Abstract

We have constructed a primary genetic map of human chromosome 18 consisting of 11 DNA markers and one serological marker (JK). Two of these loci define highly polymorphic VNTR systems. The markers define a continuous genetic linkage map of 97 cM in males and 205 cM in females; female genetic distances in a panel of 59 three-generation families were consistently about twice those observed in males. The high odds in support of the linear order of the markers on this recombination map, and the extent of coverage of chromosome 18, indicate that this map will permit efficient linkage studies of human genetic diseases that may be segregating on chromosome 18 and will provide anchor points for development of high-resolution maps for this chromosome.

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Year:  1988        PMID: 3243552     DOI: 10.1016/0888-7543(88)90129-2

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


  9 in total

1.  No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

Authors:  P Heutink; B J van de Wetering; G J Breedveld; J Weber; L A Sandkuyl; E J Devor; A Heiberg; M F Niermeijer; B A Oostra
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

2.  Parental origin of the extra chromosome in trisomy 18.

Authors:  K G Kupke; U Müller
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

3.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

4.  Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements.

Authors:  J A Armour; Z Wong; V Wilson; N J Royle; A J Jeffreys
Journal:  Nucleic Acids Res       Date:  1989-07-11       Impact factor: 16.971

5.  Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopic in situ hybridization.

Authors:  T Hori; E Takahashi; D Ayusawa; K Takeishi; S Kaneda; T Seno
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

6.  Restoration of the cholesterol metabolism in 3T3 cell lines derived from the sphingomyelinosis mouse (spm/spm) by transfer of a human chromosome 18.

Authors:  A Kurimasa; K Ohno; M Oshimura
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

7.  Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified.

Authors:  C S Cropp; R Lidereau; G Campbell; M H Champene; R Callahan
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

8.  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

9.  Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome.

Authors:  A J Pakstis; P Heutink; D L Pauls; R Kurlan; B J van de Wetering; J F Leckman; L A Sandkuyl; J R Kidd; G J Breedveld; C M Castiglione
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

  9 in total

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