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 Varnum, D. S.
Right arrow Articles by Fox, S. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Varnum, D. S.
Right arrow Articles by Fox, S. C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

The Journal of Heredity 1981:72(4):293-293
© 1981 The American Genetic Association 72:293


other

Head blebs: a new mutation on chromosome 4 of the mouse

Don S. Varnum, and Sally C. Fox

Jackson Laboratory Bar Harbor, Maine 04609.

Abstract

The developmental effects and inheritance of a new mutation in the mouse, head blebs, gene symbol heb, are described. This mutation is similar to two other autosomal recessive mutations, eb and my. Head blebs produces abnormal or missing eyes due to prenatal blebs, usually on the head, some fetal death, open eyelids, and folded retinas at birth. Extra toes or ectopic brains are occasionally observed. Affected adults usually have closed eyelids and atrophic eyes. Head blebs is located on chromosome 4, four units from pintail (Pt).


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
Proc. Natl. Acad. Sci. USAHome page
D. Kiyozumi, N. Sugimoto, and K. Sekiguchi
Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects
PNAS, August 8, 2006; 103(32): 11981 - 11986.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
I. Smyth and P. Scambler
The genetics of Fraser syndrome and the blebs mouse mutants
Hum. Mol. Genet., October 15, 2005; 14(suppl_2): R269 - R274.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
I. Smyth, X. Du, M. S. Taylor, M. J. Justice, B. Beutler, and I. J. Jackson
The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis
PNAS, September 14, 2004; 101(37): 13560 - 13565.
[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.