FASEB J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rossiter, B. J.
Right arrow Articles by Caskey, C. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rossiter, B. J.
Right arrow Articles by Caskey, C. T.

The FASEB Journal, Vol 5, 21-27, Copyright © 1991 by The Federation of American Societies for Experimental Biology


REVIEWS

Molecular studies of human genetic disease

BJ Rossiter and CT Caskey
Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.

A wide variety of techniques are available for detecting disease- causing mutations within human genes; this report provides a brief review of such procedures. Good communication and exchange of materials between the clinical genetics field and the Human Genome Initiative will benefit both.


This article has been cited by other articles:


Home page
Genome ResHome page
Y. Boyd, H. J. Blair, P. Cunliffe, W. K. Masson, and V. Reed
A Phenotype Map of the Mouse X Chromosome: Models for Human X-linked Disease
Genome Res., March 1, 2000; 10(3): 277 - 292.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1991 by The Federation of American Societies for Experimental Biology.