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Physical mapping of genetic markers on the short arm of chromosome 5.

Abstract：

:The deletion of the short arm of chromosome 5 is associated with the cri-du-chat syndrome. In addition, loss of this portion of a chromosome is a common cytogenetic marker in a number of malignancies. However, to date, no genes associated with these disorders have been identified. Physical maps are the first step in isolating causative genes, and genes involved in autosomal recessive disorders are now routinely mapped through the identification of linked markers. Extensive genetic maps based upon polymorphic short tandem repeats (STRs) have provided researchers with a large number of markers to which such disorders can be genetically mapped. However, the physical locations of many of these STRs have not been determined. Toward the goal of integrating the human genetic maps with the physical maps, a 5p somatic cell hybrid deletion mapping panel that was derived from patients with 5p deletions or translocations was used to physically map 47 STRs that have been used to construct genetic maps of 5p. These data will be useful in the localization of disease genes that map to 5p and may be involved in the etiology of the cri-du-chat syndrome.

journal_name

Genomics

journal_title

Genomics

authors

Gersh M,Goodart SA,Overhauser J

doi

10.1006/geno.1994.1668

subject

Has Abstract

pub_date

1994-12-01 00:00:00

pages

577-9

issue

3

eissn

0888-7543

issn

1089-8646

pii

S0888-7543(84)71668-5

journal_volume

24

pub_type

杂志文章

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