|
Cha, K B; Karolyi, I J; Hunt, A et al. (2004) Skeletal dysplasia and male infertility locus on mouse chromosome 9. Genomics 83:951-60
|
|
Argeson, A C; Nelson, K K; Siracusa, L D (1996) Molecular basis of the pleiotropic phenotype of mice carrying the hypervariable yellow (Ahvy) mutation at the agouti locus. Genetics 142:557-67
|
|
Siracusa, L D; McGrath, R; Ma, Q et al. (1996) A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation. Genome Res 6:300-13
|
|
Argeson, A C; Druck, T; Veronese, M L et al. (1995) Phospholipase C gamma-2 (Plcg2) and phospholipase C gamma-1 (Plcg1) map to distinct regions in the human and mouse genomes. Genomics 25:29-35
|
|
MacPhee, M; Chepenik, K P; Liddell, R A et al. (1995) The secretory phospholipase A2 gene is a candidate for the Mom1 locus, a major modifier of ApcMin-induced intestinal neoplasia. Cell 81:957-66
|
|
Pavan, W J; Liddell, R A; Wright, A et al. (1995) A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease. Mamm Genome 6:1-7
|
|
Siracusa, L D; Abbott, C M (1994) Mouse chromosome 2. Mamm Genome 5 Spec No:S22-39
|
|
Goldstein, C; Liaw, P; Jimenez, S A et al. (1994) Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome. Mamm Genome 5:696-700
|
|
Siracusa, L D; Abbott, C M (1993) Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 2. Mamm Genome 4 Spec No:S31-46
|
