Davies KE - Search Results

1

PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28.

Lindsay S, Splitt M, Edney S, Berney TP, Knight SJ, Davies KE, O'Brien O, Gale M, Burn J. Lindsay S, et al. Among authors: davies ke. Am J Hum Genet. 1996 Jun;58(6):1120-6. Am J Hum Genet. 1996. PMID: 8651288 Free PMC article.

2

Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.

Hamel BC, Smits AP, de Graaff E, Smeets DF, Schoute F, Eussen BH, Knight SJ, Davies KE, Assman-Hulsmans CF, Oostra BA. Hamel BC, et al. Among authors: davies ke. Am J Hum Genet. 1994 Nov;55(5):923-31. Am J Hum Genet. 1994. PMID: 7977354 Free PMC article.

3

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.

Lindsay S, Thiselton DL, Bateman JB, Ngo JT, Sparkes RS, Coleman M, Davies KE, Bhattacharya SS. Lindsay S, et al. Among authors: davies ke. Hum Genet. 1992 Jan;88(3):349-50. doi: 10.1007/BF00197273. Hum Genet. 1992. PMID: 1733838

4

Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap.

Knight SJ, Voelckel MA, Hirst MC, Flannery AV, Moncla A, Davies KE. Knight SJ, et al. Among authors: davies ke. Am J Hum Genet. 1994 Jul;55(1):81-6. Am J Hum Genet. 1994. PMID: 8023854 Free PMC article.

5

Dinucleotide repeat polymorphism at the DXS556 locus.

Thiselton DL, Kamakari S, Curtis AR, Coleman MP, Davies KE, Lindsay S, Bhattacharya S. Thiselton DL, et al. Among authors: davies ke. Hum Mol Genet. 1993 May;2(5):613. doi: 10.1093/hmg/2.5.613. Hum Mol Genet. 1993. PMID: 8518809 No abstract available.

6

A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.

Knight SJ, Ritchie RJ, Chakrabarti L, Cross G, Taylor GR, Mueller RF, Hurst J, Paterson J, Yates JR, Dow DJ, Davies KE. Knight SJ, et al. Among authors: davies ke. Am J Hum Genet. 1996 May;58(5):906-13. Am J Hum Genet. 1996. PMID: 8651274 Free PMC article.

7

A candidate gene for mild mental handicap at the FRAXE fragile site.

Chakrabarti L, Knight SJ, Flannery AV, Davies KE. Chakrabarti L, et al. Among authors: davies ke. Hum Mol Genet. 1996 Feb;5(2):275-82. doi: 10.1093/hmg/5.2.275. Hum Mol Genet. 1996. PMID: 8824884

8

Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28.

Ritchie RJ, Chakrabarti L, Knight SJ, Harding RM, Davies KE. Ritchie RJ, et al. Among authors: davies ke. Am J Med Genet. 1997 Dec 31;73(4):463-9. doi: 10.1002/(sici)1096-8628(19971231)73:4<463::aid-ajmg16>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9415475

9

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.

Coleman M, Bhattacharya S, Lindsay S, Wright A, Jay M, Litt M, Craig I, Davies K. Coleman M, et al. Am J Hum Genet. 1990 Dec;47(6):935-40. Am J Hum Genet. 1990. PMID: 2239970 Free PMC article.

10

The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

Ritchie RJ, Knight SJ, Hirst MC, Grewal PK, Bobrow M, Cross GS, Davies KE. Ritchie RJ, et al. Among authors: davies ke. Hum Mol Genet. 1994 Dec;3(12):2115-21. doi: 10.1093/hmg/3.12.2115. Hum Mol Genet. 1994. PMID: 7881407

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