Harding AE - Search Results

1

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I.

Jodice C, Malaspina P, Persichetti F, Novelletto A, Spadaro M, Giunti P, Morocutti C, Terrenato L, Harding AE, Frontali M. Jodice C, et al. Among authors: harding ae. Am J Hum Genet. 1994 Jun;54(6):959-65. Am J Hum Genet. 1994. PMID: 8198139 Free PMC article.

2

The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.

Giunti P, Sweeney MG, Spadaro M, Jodice C, Novelletto A, Malaspina P, Frontali M, Harding AE. Giunti P, et al. Among authors: harding ae. Brain. 1994 Aug;117 ( Pt 4):645-9. doi: 10.1093/brain/117.4.645. Brain. 1994. PMID: 7922453 Free article.

3

Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth.

Giunti P, Sweeney MG, Harding AE. Giunti P, et al. Among authors: harding ae. Brain. 1995 Oct;118 ( Pt 5):1077-85. doi: 10.1093/brain/118.5.1077. Brain. 1995. PMID: 7496771

4

The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.

David G, Giunti P, Abbas N, Coullin P, Stevanin G, Horta W, Gemmill R, Weissenbach J, Wood N, Cunha S, Drabkin H, Harding AE, Agid Y, Brice A. David G, et al. Among authors: harding ae. Am J Hum Genet. 1996 Dec;59(6):1328-36. Am J Hum Genet. 1996. PMID: 8940279 Free PMC article.

5

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.

La Spada AR, Roling DB, Harding AE, Warner CL, Spiegel R, Hausmanowa-Petrusewicz I, Yee WC, Fischbeck KH. La Spada AR, et al. Among authors: harding ae. Nat Genet. 1992 Dec;2(4):301-4. doi: 10.1038/ng1292-301. Nat Genet. 1992. PMID: 1303283

6

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

Sweeney MG, Davis MB, Lashwood A, Brockington M, Toscano A, Harding AE. Sweeney MG, et al. Among authors: harding ae. Am J Hum Genet. 1992 Oct;51(4):741-8. Am J Hum Genet. 1992. PMID: 1415219 Free PMC article.

7

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Chalmers RM, Davis MB, Sweeney MG, Wood NW, Harding AE. Chalmers RM, et al. Among authors: harding ae. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.

8

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

Harding AE, Sweeney MG, Govan GG, Riordan-Eva P. Harding AE, et al. Am J Hum Genet. 1995 Jul;57(1):77-86. Am J Hum Genet. 1995. PMID: 7611298 Free PMC article.

9

Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q.

Chamberlain S, Farrall M, Shaw J, Wilkes D, Carvajal J, Hillerman R, Doudney K, Harding AE, Williamson R, Sirugo G, et al. Chamberlain S, et al. Among authors: harding ae. Am J Hum Genet. 1993 Jan;52(1):99-109. Am J Hum Genet. 1993. PMID: 8434613 Free PMC article.

10

Mitochondrial DNA polymorphism in mitochondrial myopathy.

Holt IJ, Harding AE, Morgan-Hughes JA. Holt IJ, et al. Among authors: harding ae. Hum Genet. 1988 May;79(1):53-7. doi: 10.1007/BF00291710. Hum Genet. 1988. PMID: 2896621

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

251 results

Search Page

Filters