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PMID: 6587566 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11.

Science (New York, N.Y.) ·Vol. 225 ·No. 4657 ·1984-07-06 ·Pages 57-9

Lebo RV, Gorin F, Fletterick RJ, Kao FT, Cheung MC, Bruce BD, Kan YW

Abstract

A rapid gene-mapping system uses a high-resolution, dual-laser sorter to identify genes from separate human chromosomes prepared with a new stain combination. This system was used to sort 21 unique chromosome types onto nitrocellulose filter papers. Several labeled gene probes hybridized to the sorted chromosomal DNA types predicted by their previous chromosome assignments. The skeletal muscle glycogen phosphorylase gene was then mapped to a portion of chromosome 11 by spot blotting normal and translocated chromosomes.

MeSH Terms
Animals Chromosome Mapping Chromosomes, Human, 6-12 and X Cricetinae Cricetulus DNA/metabolism Glycogen Storage Disease/genetics Glycogen Storage Disease Type V/genetics Humans Hybrid Cells Karyotyping Male Nucleic Acid Hybridization Phosphorylases/genetics
Chemicals
DNA Phosphorylases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Lebo R V
Gorin F
Fletterick R J
Kao F T
Cheung M C
Bruce B D
Kan Y W
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1984-07-06
Pages
57-9
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIADDK NIH HHS · AM32822 · United States
NICHD NIH HHS · HD02081 · United States
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