Skip Navigation

This Article
Right arrow Full Text (PDF)
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 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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Nieuwenhuijsen, B.W.
Right arrow Articles by Fischbeck, V.H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nieuwenhuijsen, B.W.
Right arrow Articles by Fischbeck, V.H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1992 Oxford University Press

OTHER

A yeast artificial chromosome contig spanning the Charcot — Marie — Tooth disease type 1A duplication region

B.W. Nieuwenhuijsen, K.L. Chen, A.C. Chinault1, S. Wang, V.H. Valmiki, E.J. Meershoek2, G.J.B. van Ommen2 and V.H. Fischbeck*

Department of Neurology, University of Pennsylvania, School of Medicine 422 Curie Boulevard, Philadelphia, PA 19104-6146 1Institute for Molecular Genetics and Human Genome Center, One Baylor Plaza, Baylor College of Medicine Houston, TX 77030, USA 2Department of Human Genetics, State University of Leiden, Sylvius Laboratories Wassenaarseweg 72, 2333 AL Leiden, The Netherlands

* To whom correspondence should be addressed

Received July 20, 1992; Revised September 4, 1992; Accepted September 4, 1992

A contiguous set of 43 overlapping yeast artificial chromosome (YAC) clones has been developed for the Charcot—Marie—Tooth disease type 1A (CMT1A) duplication region of chromosome 17p11.2. The contig spans approximately 2.0 Mb and can be represented in a minimum of five overlapping YACs. The YAC clones were isolated from two total human genomic YAC libraries and from YAC libraries made from rodent-human hybrid cell lines. YAC clones were isolated from the libraries by polymerase chain reaction (PCR) technique. Localization to chromosome 17p11.2 was confirmed by fluorescence in situ hybridization. Overlap between the YAC clones was detected by inter-Alu PCR amplification of the YACs and by cross hybridization of the YACs with YAC insert ends obtained by Vectorette PCR. This YAC contig is a useful resource for analyzing and mapping all the genes contained within the CMT1A duplication.


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




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.