Davies KE - Search Results

1

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

Kenwrick S, Ionasescu V, Ionasescu G, Searby C, King A, Dubowitz M, Davies KE. Kenwrick S, et al. Among authors: davies ke. Hum Genet. 1986 Jul;73(3):264-6. doi: 10.1007/BF00401241. Hum Genet. 1986. PMID: 3460961

2

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.

Read AP, Thakker RV, Davies KE, Mountford RC, Brenton DP, Davies M, Glorieux F, Harris R, Hendy GN, King A, et al. Read AP, et al. Among authors: davies ke, davies m. Hum Genet. 1986 Jul;73(3):267-70. doi: 10.1007/BF00401242. Hum Genet. 1986. PMID: 3015770

3

Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.

Thibodeau SN, Dorkins HR, Faulk KR, Berry R, Smith AC, Hagerman R, King A, Davies KE. Thibodeau SN, et al. Among authors: davies ke. Hum Genet. 1988 Jul;79(3):219-27. doi: 10.1007/BF00366240. Hum Genet. 1988. PMID: 3402993

4

A study of genetic linkage heterogeneity in adult polycystic kidney disease.

Reeders ST, Breuning MH, Ryynanen MA, Wright AF, Davies KE, King AW, Watson ML, Weatherall DJ. Reeders ST, et al. Among authors: davies ke. Hum Genet. 1987 Aug;76(4):348-51. doi: 10.1007/BF00272443. Hum Genet. 1987. PMID: 3610154

5

Patterns of exon deletions in Duchenne and Becker muscular dystrophy.

Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Davies KE, Harris R. Read AP, et al. Among authors: davies ke. Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859. Hum Genet. 1988. PMID: 3169738

6

Molecular analysis of human X-linked diseases.

Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, King AW, Lavenir IJ, McGlade SA, Patterson MN, Smith TJ, et al. Davies KE, et al. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:337-43. doi: 10.1101/sqb.1986.051.01.039. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3472730 No abstract available.

7

Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy.

Davies KE, Briand P, Ionasescu V, Ionasescu G, Williamson R, Brown C, Cavard C, Cathelineau L. Davies KE, et al. Nucleic Acids Res. 1985 Jan 11;13(1):155-65. doi: 10.1093/nar/13.1.155. Nucleic Acids Res. 1985. PMID: 3839070 Free PMC article.

8

Bridging markers defining the map position of X linked hypophosphataemic rickets.

Thakker RV, Read AP, Davies KE, Whyte MP, Weksberg R, Glorieux F, Davies M, Mountford RC, Harris R, King A, et al. Thakker RV, et al. Among authors: davies ke, davies m. J Med Genet. 1987 Dec;24(12):756-60. doi: 10.1136/jmg.24.12.756. J Med Genet. 1987. PMID: 2828625 Free PMC article.

9

Localization of the gene for X-linked spinal muscular atrophy.

Fischbeck KH, Ionasescu V, Ritter AW, Ionasescu R, Davies K, Ball S, Bosch P, Burns T, Hausmanowa-Petrusewicz I, Borkowska J, et al. Fischbeck KH, et al. Neurology. 1986 Dec;36(12):1595-8. doi: 10.1212/wnl.36.12.1595. Neurology. 1986. PMID: 3466055

10

Molecular analysis of human muscular dystrophies.

Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M. Davies KE, et al. Muscle Nerve. 1987 Mar-Apr;10(3):191-9. doi: 10.1002/mus.880100302. Muscle Nerve. 1987. PMID: 2882417 Review.

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