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The mouse mutation ulnaless on chromosome 2.

作者信息

Davisson M T, Cattanach B M

机构信息

Jackson Laboratory, Bar Harbor, Maine 04609.

出版信息

J Hered. 1990 Mar-Apr;81(2):151-3.

PMID:2338491
Abstract

The dominant skeletal mutation ulnaless (Ul) in the mouse causes extreme reduction of the radius and ulna and deformities of the tibia and fibula. Penetrance appears to be complete, but the homozygote is not known, as heterozygous males do not breed. We report the linkage of the Ul gene on Chromosome 2, 18 cM proximal to pallid (pa), and describe its phenotypic effects.

摘要

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