Patterson MN - Search Results

1

Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.

Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B, et al. Patterson MN, et al. Genomics. 1989 May;4(4):570-8. doi: 10.1016/0888-7543(89)90281-4. Genomics. 1989. PMID: 2744766

2

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: patterson mn. Am J Med Genet. 1991 Feb-Mar;38(2-3):354-6. doi: 10.1002/ajmg.1320380238. Am J Med Genet. 1991. PMID: 1673311

3

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: patterson mn. Genomics. 1991 May;10(1):243-9. doi: 10.1016/0888-7543(91)90506-a. Genomics. 1991. PMID: 2045104

4

Physical mapping of DXS134 close to the DXS52 locus.

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

5

Molecular analysis of the fragile X syndrome.

Froster-Iskenius U, Patterson MN, Bell MV, Bloomfield J, Davies KE. Froster-Iskenius U, et al. Among authors: patterson mn. Q J Med. 1988 Oct;68(258):755-63. Q J Med. 1988. PMID: 3077469 Review. No abstract available.

6

Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.

Patterson M, Bell M, Schwartz C, Davies K. Patterson M, et al. Am J Med Genet. 1988 May-Jun;30(1-2):581-91. doi: 10.1002/ajmg.1320300159. Am J Med Genet. 1988. PMID: 3177471

7

Physical mapping studies on the human X chromosome in the region Xq27-Xqter.

Patterson M, Schwartz C, Bell M, Sauer S, Hofker M, Trask B, van den Engh G, Davies KE. Patterson M, et al. Genomics. 1987 Dec;1(4):297-306. doi: 10.1016/0888-7543(87)90028-0. Genomics. 1987. PMID: 3482420

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. Am J Hum Genet. 1989 May;44(5):679-85. Am J Hum Genet. 1989. PMID: 2565080 Free PMC article.

9

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. Among authors: patterson mn. Am J Hum Genet. 1989 Dec;45(6):883-8. Am J Hum Genet. 1989. PMID: 2574000 Free PMC article.

10

Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.

Davies KE, Patterson MN, Kenwrick SJ, Bell MV, Sloan HR, Westman JA, Elsas LJ 2nd, Mahan J. Davies KE, et al. Among authors: patterson mn. Am J Med Genet. 1988 Mar;29(3):557-64. doi: 10.1002/ajmg.1320290313. Am J Med Genet. 1988. PMID: 2837087

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