|
Chi, H; Tiller, G E; Dasouki, M J et al. (1999) Multiple inositol polyphosphate phosphatase: evolution as a distinct group within the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19. Genomics 56:324-36
|
|
Tiller, G E; Warman, M L; Gong, Y et al. (1998) Physical and linkage mapping of the gene for the alpha3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3. Cytogenet Cell Genet 81:205-7
|
|
Griffith, A J; Sprunger, L K; Sirko-Osadsa, D A et al. (1998) Marshall syndrome associated with a splicing defect at the COL11A1 locus. Am J Hum Genet 62:816-23
|
|
Croop, J M; Tiller, G E; Fletcher, J A et al. (1997) Isolation and characterization of a mammalian homolog of the Drosophila white gene. Gene 185:77-85
|
|
Tiller, G E; Polumbo, P A; Weis, M A et al. (1995) Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick type. Nat Genet 11:87-9
|
|
Vikkula, M; Mariman, E C; Lui, V C et al. (1995) Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus. Cell 80:431-7
|
|
Tiller, G E; Weis, M A; Polumbo, P A et al. (1995) An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenita. Am J Hum Genet 56:388-95
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