Literature DB >> 8276418

High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1.

N Van Roy1, G Laureys, R Versteeg, G Opdenakker, F Speleman.   

Abstract

We describe a high-resolution cytogenetic map for 46 DNA markers previously assigned to the short arm of human chromosome 1. Using fluorescence in situ hybridization on simultaneously R-banded prometaphase chromosomes, a refined map position was found for 45 probes. For 6 of these probes, additional hybridization sites were observed and for another 7 probes, conflicting results were found with regard to previous localizations. For some probes with overlapping map positions, probe order could be determined by dual-color hybridization on elongated chromosomes. The present high-resolution map can be used to refine the previously published composite map and also provides additional landmarks for the construction of a contig map of the short arm of chromosomes 1.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8276418     DOI: 10.1006/geno.1993.1427

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


  7 in total

1.  Duplication of seven exons in the lysyl hydroxylase gene is associated with longer forms of a repetitive sequence within the gene and is a common cause for the type VI variant of Ehlers-Danlos syndrome.

Authors:  J Heikkinen; T Toppinen; H Yeowell; T Krieg; B Steinmann; K I Kivirikko; R Myllylä
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

2.  Localization of the gene encoding a novel isoform of lysyl hydroxylase.

Authors:  C Szpirer; J Szpirer; M Rivière; P Vanvooren; M Valtavaara; R Myllylä
Journal:  Mamm Genome       Date:  1997-09       Impact factor: 2.957

3.  Chromosome mapping of the rat phospholipase C beta 1 gene.

Authors:  G Calabrese; R S Gilmour; L Stuppia; R Di Pietro; G Palka; L Cocco
Journal:  Mamm Genome       Date:  1995-08       Impact factor: 2.957

4.  Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.

Authors:  H Caron; P van Sluis; N van Roy; J de Kraker; F Speleman; P A Voûte; A Westerveld; R Slater; R Versteeg
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

5.  Alu-Alu recombination results in a duplication of seven exons in the lysyl hydroxylase gene in a patient with the type VI variant of Ehlers-Danlos syndrome.

Authors:  B Pousi; T Hautala; J Heikkinen; L Pajunen; K I Kivirikko; R Myllylä
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

6.  A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.

Authors:  P S White; J M Maris; C Beltinger; E Sulman; H N Marshall; M Fujimori; B A Kaufman; J A Biegel; C Allen; C Hilliard; M B Valentine; A T Look; H Enomoto; S Sakiyama; G M Brodeur
Journal:  Proc Natl Acad Sci U S A       Date:  1995-06-06       Impact factor: 11.205

7.  Elongated mouse chromosomes suitable for enhanced molecular cytogenetics.

Authors:  Sherif Louis; Katalin Benedek; Michael Mowat; George Klein; Sabine Mai
Journal:  Cytotechnology       Date:  2004-03       Impact factor: 2.058

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.