Byth BC - 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: byth bc. Am J Med Genet. 1993 Apr 15;46(2):172-5. doi: 10.1002/ajmg.1320460214. Am J Med Genet. 1993. PMID: 8484404

2

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. J Neurol Sci. 1991 Apr;102(2):206-8. doi: 10.1016/0022-510x(91)90070-n. J Neurol Sci. 1991. PMID: 1883411

3

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. Cytogenet Cell Genet. 1992;60(3-4):216-8. doi: 10.1159/000133342. Cytogenet Cell Genet. 1992. PMID: 1354595

4

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. 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.

5

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: byth bc. Hum Mol Genet. 1993 Nov;2(11):1765-72. doi: 10.1093/hmg/2.11.1765. Hum Mol Genet. 1993. PMID: 8281135

6

Dystrophin and dystrophin-related proteins: a review of protein and RNA studies.

Love DR, Byth BC, Tinsley JM, Blake DJ, Davies KE. Love DR, et al. Among authors: byth bc. Neuromuscul Disord. 1993 Jan;3(1):5-21. doi: 10.1016/0960-8966(93)90037-k. Neuromuscul Disord. 1993. PMID: 8329888 Review.

7

An autosomal transcript in skeletal muscle with homology to dystrophin.

Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, Marsden RF, Walsh FS, Edwards YH, Davies KE. Love DR, et al. Among authors: byth bc. Nature. 1989 May 4;339(6219):55-8. doi: 10.1038/339055a0. Nature. 1989. PMID: 2541343

8

Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.

Byth BC, Costa MT, Teshima IE, Wilson WG, Carter NP, Cox DW. Byth BC, et al. J Med Genet. 1995 Jul;32(7):564-7. doi: 10.1136/jmg.32.7.564. J Med Genet. 1995. PMID: 7562974 Free PMC article.

9

Physical and genetic mapping of the serpin gene cluster at 14q32.1: allelic association and a unique haplotype associated with alpha 1-antitrypsin deficiency.

Byth BC, Billingsley GD, Cox DW. Byth BC, et al. Am J Hum Genet. 1994 Jul;55(1):126-33. Am J Hum Genet. 1994. PMID: 7912884 Free PMC article.

10

Polymorphism of the protein C inhibitor (PCI) gene on chromosome 14.

Ashbourne KJ, Byth BC, Meijers JC, Cox DW. Ashbourne KJ, et al. Among authors: byth bc. Hum Mol Genet. 1993 Jan;2(1):92. doi: 10.1093/hmg/2.1.92. Hum Mol Genet. 1993. PMID: 8098248 No abstract available.

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