The original shaker-with-syndactylism mutation ( sy ) is a contiguous gene deletion syndrome
- 1 November 1998
- journal article
- research article
- Published by Springer Nature in Mammalian Genome
- Vol. 9 (11) , 889-892
- https://doi.org/10.1007/s003359900889
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Serrate2 is disrupted in the mouse limb-development mutant syndactylismNature, 1997
- mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)Genomics, 1997
- A type VII myosin encoded by the mouse deafness gene shaker-1Nature, 1995
- Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouseMammalian Genome, 1994
- A Macintosh program for storage and analysis of experimental genetic mapping dataMammalian Genome, 1993
- Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5.Proceedings of the National Academy of Sciences, 1991
- Mutations induced by X-rays at the HPRT locus in cultured Chinese hamster cells are mostly large deletionsMutation Research Letters, 1985
- Chromosome 18 of the house mouseJournal of Heredity, 1981
- The Development of the Inner Ear in Mice Homozygous for Shaker-with-SyndactylismDevelopment, 1963