Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (2)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Hall, E. H.
Right arrow Articles by King, T. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hall, E. H.
Right arrow Articles by King, T. R.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

The Journal of Heredity 2000:91(4)
© 2000 The American Genetic Association 91:345-347

Brief communication. The hypotrichosis-generating shorn (shn) mutation maps to distal chromosome 7 in the Norway rat

EH Hall, JA Lathrop, B Medina, RJ Mutcherson, II, and TR King*

Department of Biological Sciences, Central Connecticut State University, 1615 Stanley St., New Britain, CT 06050, USA *Corresponding author

We have recently identified an autosomal recessive mutation in the Norway rat that generates an almost complete absence of normal hair. Here we describe a multilocus backcross analysis that was used to map this mutation, named shorn (gene symbol shn), to the distal end of rat chromosome 7. Although this region in rat carries no previously mapped similar mutations, the homologous genomic regions in mouse and human contain several potential homologues and candidate genes.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
 J HeredHome page
K. Ahearn, G. Akkouris, P. R. Berry, R. R. Chrissluis, I. M. Crooks, A. K. Dull, S. Grable, J. Jeruzal, J. Lanza, C. Lavoie, et al.
The Charles River "Hairless" Rat Mutation Maps to Chromosome 1: Allelic With Fuzzy and a Likely Orthologue of Mouse Frizzy
J. Hered., May 1, 2002; 93(3): 210 - 213.
[Abstract] [Full Text] [PDF]


Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.