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
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).
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||

