Davies KE - Search Results

1

Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.

Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Passos-Bueno MR, et al. Among authors: davies ke. Am J Med Genet. 1991 Jan;38(1):140-6. doi: 10.1002/ajmg.1320380130. Am J Med Genet. 1991. PMID: 2012126

2

Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy.

Love DR, Flint TJ, Genet SA, Middleton-Price HR, Davies KE. Love DR, et al. Among authors: davies ke. J Med Genet. 1991 Dec;28(12):860-4. doi: 10.1136/jmg.28.12.860. J Med Genet. 1991. PMID: 1757963 Free PMC article.

3

Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27.

Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Passos-Bueno MR, et al. Among authors: davies ke. J Neurol Sci. 1991 Apr;102(2):206-8. doi: 10.1016/0022-510x(91)90070-n. J Neurol Sci. 1991. PMID: 1883411

4

Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.

Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Passos-Bueno MR, et al. Among authors: davies ke. J Med Genet. 1990 Mar;27(3):145-50. doi: 10.1136/jmg.27.3.145. J Med Genet. 1990. PMID: 2182872 Free PMC article.

5

Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M. Passos-Bueno MR, et al. Among authors: davies ke. Am J Med Genet. 1993 Apr 15;46(2):172-5. doi: 10.1002/ajmg.1320460214. Am J Med Genet. 1993. PMID: 8484404

6

Localization of two new DNA markers on the linkage map of human chromosome 6q.

Byth BC, Love DR, Murray JC, Davies KE. Byth BC, et al. Among authors: davies ke. Cytogenet Cell Genet. 1992;60(3-4):216-8. doi: 10.1159/000133342. Cytogenet Cell Genet. 1992. PMID: 1354595

7

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus.

Buckle VJ, Guenet JL, Simon-Chazottes D, Love DR, Davies KE. Buckle VJ, et al. Among authors: davies ke. Hum Genet. 1990 Aug;85(3):324-6. doi: 10.1007/BF00206755. Hum Genet. 1990. PMID: 2203673

8

Characterization of deletions in the dystrophin gene giving mild phenotypes.

Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Love DR, et al. Among authors: davies ke. Am J Med Genet. 1990 Sep;37(1):136-42. doi: 10.1002/ajmg.1320370132. Am J Med Genet. 1990. PMID: 2240031

9

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.

England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. England SB, et al. Among authors: davies ke. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

10

Duchenne muscular dystrophy: the gene and the protein.

Love DR, Davies KE. Love DR, et al. Among authors: davies ke. Mol Biol Med. 1989 Feb;6(1):7-17. Mol Biol Med. 1989. PMID: 2666821 Review. No abstract available.

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