Bell M - Search Results

1

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A. Davies KE, et al. Among authors: bell m. J Med Genet. 1988 Jan;25(1):9-13. doi: 10.1136/jmg.25.1.9. J Med Genet. 1988. PMID: 3162536 Free PMC article.

2

The fragile X syndrome.

Hirst MC, Knight SJ, Bell MV, Super M, Davies KE. Hirst MC, et al. Among authors: bell mv. Clin Sci (Lond). 1992 Sep;83(3):255-64. doi: 10.1042/cs0830255. Clin Sci (Lond). 1992. PMID: 1327643

3

Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers.

Glass IA, Pirrit LA, White EM, Bell MV, Davies KE, Cockburn F, Connor JM. Glass IA, et al. Among authors: bell mv. Am J Med Genet. 1991 Feb-Mar;38(2-3):298-304. doi: 10.1002/ajmg.1320380227. Am J Med Genet. 1991. PMID: 1673301

4

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site.

Hirst MC, Bell MV, MacKinnon RN, Watson JE, Callen D, Sutherland G, Dahl N, Patterson MN, Schwartz C, Ledbetter D, et al. Hirst MC, et al. Among authors: bell mv. Am J Med Genet. 1991 Feb-Mar;38(2-3):354-6. doi: 10.1002/ajmg.1320380238. Am J Med Genet. 1991. PMID: 1673311

5

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.

Bell MV, Hirst MC, Nakahori Y, MacKinnon RN, Roche A, Flint TJ, Jacobs PA, Tommerup N, Tranebjaerg L, Froster-Iskenius U, et al. Bell MV, et al. Cell. 1991 Feb 22;64(4):861-6. doi: 10.1016/0092-8674(91)90514-y. Cell. 1991. PMID: 1997211

6

Linear order of new and established DNA markers around the fragile site at Xq27.3.

Hirst MC, Roche A, Flint TJ, MacKinnon RN, Bassett JH, Nakahori Y, Watson JE, Bell MV, Patterson MN, Boyd Y, et al. Hirst MC, et al. Among authors: bell mv. Genomics. 1991 May;10(1):243-9. doi: 10.1016/0888-7543(91)90506-a. Genomics. 1991. PMID: 2045104

7

Microdissection of the fragile X region.

MacKinnon RN, Hirst MC, Bell MV, Watson JE, Claussen U, Ludecke HJ, Senger G, Horsthemke B, Davies KE. MacKinnon RN, et al. Among authors: bell mv. Am J Hum Genet. 1990 Aug;47(2):181-6. Am J Hum Genet. 1990. PMID: 2378345 Free PMC article.

8

An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767).

Patterson M, Gitschier J, Bloomfield J, Bell M, Dorkins H, Froster-Iskenius U, Sommer S, Sobell J, Schaid D, Thibodeau S, et al. Patterson M, et al. Among authors: bell m. Am J Hum Genet. 1989 May;44(5):679-85. Am J Hum Genet. 1989. PMID: 2565080 Free PMC article.

9

Physical mapping of DXS134 close to the DXS52 locus.

Bell MV, Patterson MN, Dorkins HR, Davies KE. Bell MV, et al. Hum Genet. 1989 Apr;82(1):27-30. doi: 10.1007/BF00288266. Hum Genet. 1989. PMID: 2565864

10

Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.

Bell MV, Bloomfield J, McKinley M, Patterson MN, Darlison MG, Barnard EA, Davies KE. Bell MV, et al. Am J Hum Genet. 1989 Dec;45(6):883-8. Am J Hum Genet. 1989. PMID: 2574000 Free PMC article.

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