Guarnieri, Mary H; Cacheiro, Nestor L; Rudofsky, Ulrich H et al. (2002) A chromosomal translocation causing multiple abnormalities including open eyelids at birth and glomerulonephritis. Mamm Genome 13:416-22
|
Herron, B J; Bryda, E C; Heverly, S A et al. (1999) Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome 10:864-9
|
Ji, W; Herron, B; Jones, J M et al. (1999) Identification of genes within the Krd deletion on mouse chromosome 19. Mamm Genome 10:399-401
|
Qu, S; Tucker, S C; Ehrlich, J S et al. (1998) Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly. Development 125:2711-21
|
Flaherty, L (1998) Generation, identification, and recovery of mouse mutations. Methods 14:107-18
|
Kuster, J E; Guarnieri, M H; Ault, J G et al. (1997) IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa. Mamm Genome 8:673-81
|
Bryda, E C; Ling, H; Flaherty, L (1997) A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer. Mamm Genome 8:1-4
|
Baldocchi, R A; Flaherty, L (1997) Isolation of genomic fragments from polymorphic regions by representational difference analysis. Methods 13:337-46
|
Royaux, I; Bernier, B; Montgomery, J C et al. (1997) Reln(rl-Alb2), an allele of reeler isolated from a chlorambucil screen, is due to an IAP insertion with exon skipping. Genomics 42:479-82
|
Caldarone, B; Saavedra, C; Tartaglia, K et al. (1997) Quantitative trait loci analysis affecting contextual conditioning in mice. Nat Genet 17:335-7
|
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