Westbrook CA - Search Results

1

Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.

Speer MC, Gilchrist JM, Chutkow JG, McMichael R, Westbrook CA, Stajich JM, Jorgenson EM, Gaskell PC, Rosi BL, Ramesar R, et al. Speer MC, et al. Among authors: westbrook ca. Am J Hum Genet. 1995 Dec;57(6):1371-6. Am J Hum Genet. 1995. PMID: 8533766 Free PMC article.

2

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

Speer MC, Gilchrist JM, Stajich JM, Gaskell PC, Westbrook CA, Horrigan SK, Bartoloni L, Yamaoka LH, Scott WK, Pericak-Vance MA. Speer MC, et al. Among authors: westbrook ca. J Med Genet. 1998 Apr;35(4):305-8. doi: 10.1136/jmg.35.4.305. J Med Genet. 1998. PMID: 9598725 Free PMC article.

3

Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.

Speer MC, Vance JM, Lennon-Graham F, Stajich JM, Viles KD, Gilchrist JM, Nigro V, McMichael R, Chutkow JG, Bartoloni L, Horrigan SK, Westbrook CA, Pericak-Vance MA. Speer MC, et al. Among authors: westbrook ca. Hum Hered. 1998 Jul-Aug;48(4):179-84. doi: 10.1159/000022799. Hum Hered. 1998. PMID: 9694248

4

Myotilin is mutated in limb girdle muscular dystrophy 1A.

Hauser MA, Horrigan SK, Salmikangas P, Torian UM, Viles KD, Dancel R, Tim RW, Taivainen A, Bartoloni L, Gilchrist JM, Stajich JM, Gaskell PC, Gilbert JR, Vance JM, Pericak-Vance MA, Carpen O, Westbrook CA, Speer MC. Hauser MA, et al. Among authors: westbrook ca. Hum Mol Genet. 2000 Sep 1;9(14):2141-7. doi: 10.1093/hmg/9.14.2141. Hum Mol Genet. 2000. PMID: 10958653

5

Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.

Yamaoka LH, Westbrook CA, Speer MC, Gilchrist JM, Jabs EW, Schweins EG, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA. Yamaoka LH, et al. Among authors: westbrook ca. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):471-5. doi: 10.1016/0960-8966(94)90086-8. Neuromuscul Disord. 1994. PMID: 7881291

6

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 5q31.

Bartoloni L, Horrigan SK, Viles KD, Gilchrist JM, Stajich JM, Vance JM, Yamaoka LH, Pericak-Vance MA, Westbrook CA, Speer MC. Bartoloni L, et al. Among authors: westbrook ca. Genomics. 1998 Dec 1;54(2):250-5. doi: 10.1006/geno.1998.5579. Genomics. 1998. PMID: 9828127

7

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 sequences.

Horrigan SK, Bartoloni L, Speer MC, Fulton N, Kravarusic J, Ramesar R, Vance JM, Yamaoka LH, Westbrook CA. Horrigan SK, et al. Among authors: westbrook ca. Genomics. 1999 Apr 1;57(1):24-35. doi: 10.1006/geno.1999.5765. Genomics. 1999. PMID: 10191080

8

Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain.

Westbrook CA, Le Beau MM, Neuman WL, Keinanen M, Yamaoka LH, Speer MC, Espinosa R 3rd, Nakamura Y, Williamson R, Mullan M, et al. Westbrook CA, et al. Cytogenet Cell Genet. 1994;67(2):86-93. doi: 10.1159/000133805. Cytogenet Cell Genet. 1994. PMID: 7913678

9

Molecular genetics improves the management of hereditary non-polyposis colorectal cancer.

Ramesar RS, Madden MV, Felix R, Harocopos CJ, Westbrook CA, Jones G, Cruse JP, Goldberg PA. Ramesar RS, et al. Among authors: westbrook ca. S Afr Med J. 2000 Jul;90(7):709-14. S Afr Med J. 2000. PMID: 10985134

10

In a resource-poor country, mutation identification has the potential to reduce the cost of family management for hereditary nonpolyposis colorectal cancer.

Goldberg PA, Madden MV, Harocopos C, Felix R, Westbrook C, Ramesar RS. Goldberg PA, et al. Dis Colon Rectum. 1998 Oct;41(10):1250-3; discussion 1253-5. doi: 10.1007/BF02258223. Dis Colon Rectum. 1998. PMID: 9788388

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