Davies KE - Search Results

1

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

2

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

3

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.

4

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

5

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

6

A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q.

Byth BC, Love DR, Passos-Bueno MR, Davies KE. Byth BC, et al. Among authors: davies ke. Nucleic Acids Res. 1991 Aug 11;19(15):4310. doi: 10.1093/nar/19.15.4310-a. Nucleic Acids Res. 1991. PMID: 1678512 Free PMC article.

7

The utrophin and dystrophin genes share similarities in genomic structure.

Pearce M, Blake DJ, Tinsley JM, Byth BC, Campbell L, Monaco AP, Davies KE. Pearce M, et al. Among authors: davies ke. Hum Mol Genet. 1993 Nov;2(11):1765-72. doi: 10.1093/hmg/2.11.1765. Hum Mol Genet. 1993. PMID: 8281135

8

DNA studies of X-linked mental retardation associated with a fragile site at Xq27.

Davies KE. Davies KE. Am J Med Genet. 1986 Jan-Feb;23(1-2):633-42. doi: 10.1002/ajmg.1320230157. Am J Med Genet. 1986. PMID: 3513572 Review.

9

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.

Bakker E, Hofker MH, Goor N, Mandel JL, Wrogemann K, Davies KE, Kunkel LM, Willard HF, Fenton WA, Sandkuyl L, et al. Bakker E, et al. Among authors: davies ke. Lancet. 1985 Mar 23;1(8430):655-8. doi: 10.1016/s0140-6736(85)91325-x. Lancet. 1985. PMID: 2858615

10

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.

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