Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1

Author:

Brown Kathryn A.,Sutcliffe Maxine J.,Steel Karen P.,Brown Stephen D.M.

Publisher

Elsevier BV

Subject

Genetics

Reference23 articles.

1. Reverse genetic approaches to cloning deafness genes;Brown;Ann. N.Y. Acad. Sci,1991

2. Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data;Cavalli-Sforza;Am. J. Hum. Genet,1986

3. Family studies of early childhood deafness ascertained through the Clarke School for the Deaf;Chung;Am. J. Hum. Genet,1970

4. The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse;Deol,1956

5. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity;Feinberg;Anal. Biochem,1984

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4. The role of mouse mutants in the identification of human hereditary hearing loss genes;Hearing Research;1999-04

5. The MurinePolycomb-Group Geneeedand Its Human Orthologue: Functional Implications of Evolutionary Conservation;Genomics;1998-11

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