Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesSPEER, M. C; VANCE, J. M; HORRIGAN, S. K et al.Human heredity. 1998, Vol 48, Num 4, pp 179-184, issn 0001-5652Article

Human mortalin (HSPA9) : a candidate for the myeloid leukemia tumor suppressor gene on 5q31XIE, H; HU, Z; CHYNA, B et al.Leukemia. 2000, Vol 14, Num 12, pp 2128-2134, issn 0887-6924Article

The Smad5 gene is involved in the intracellular signaling pathways that mediate the inhibitory effects of transforming growth factor-β on human hematopoiesisBRUNO, E; HORRIGAN, S. K; VAN DEN BERG, D et al.Blood. 1998, Vol 91, Num 6, pp 1917-1923, issn 0006-4971Article

A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesHORRIGAN, S. K; BARTOLONI, L; SPEER, M. C et al.Genomics (San Diego, Calif.). 1999, Vol 57, Num 1, pp 24-35, issn 0888-7543Article

Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31BARTOLONI, L; HORRIGAN, S. K; VILES, K. D et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 2, pp 250-255, issn 0888-7543Article

Characterization of an associated microfibril protein through recombinant DNA techniquesHORRIGAN, S. K; RICH, C. B; STREETEN, B. W et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 14, pp 10087-10095, issn 0021-9258Article

Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasiaWESTBROOK, C. A; HSU, W.-T; CHYNA, B et al.British journal of haematology. 2000, Vol 110, Num 4, pp 847-855, issn 0007-1048Article

Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31HORRIGAN, S. K; ARBIEVA, Z. H; HONG YAN XIE et al.Blood. 2000, Vol 95, Num 7, pp 2372-2377, issn 0006-4971Article

Myotilin is mutated in limb girdle muscular dystrophy 1AHAUSER, M. A; HORRIGAN, S. K; STAJICH, J. M et al.Human molecular genetics (Print). 2000, Vol 9, Num 14, pp 2141-2147, issn 0964-6906Article

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophySPEER, M. C; GILCHRIST, J. M; STAJICH, J. M et al.Journal of medical genetics. 1998, Vol 35, Num 4, pp 305-308, issn 0022-2593Article

Polymerase chain reaction-based diagnosis of Del(5q) in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion intervalHORRIGAN, S. K; WESTBROOK, C. A; KIM, A. H et al.Blood. 1996, Vol 88, Num 7, pp 2665-2670, issn 0006-4971Article