Farrall M - Search Results

1

Genetic homogeneity at the Friedreich ataxia locus on chromosome 9.

Chamberlain S, Shaw J, Wallis J, Rowland A, Chow L, Farrall M, Keats B, Richter A, Roy M, Melancon S, et al. Chamberlain S, et al. Among authors: farrall m. Am J Hum Genet. 1989 Apr;44(4):518-21. Am J Hum Genet. 1989. PMID: 2929596 Free PMC article.

2

Prenatal diagnosis of Friedreich ataxia.

Wallis J, Shaw J, Wilkes D, Farrall M, Williamson R, Chamberlain S, Skare JC, Milunsky A. Wallis J, et al. Among authors: farrall m. Am J Med Genet. 1989 Nov;34(3):458-61. doi: 10.1002/ajmg.1320340327. Am J Med Genet. 1989. PMID: 2574535

3

Mapping of mutation causing Friedreich's ataxia to human chromosome 9.

Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, von Gabain A, Farrall M, Williamson R. Chamberlain S, et al. Among authors: farrall m. Nature. 1988 Jul 21;334(6179):248-50. doi: 10.1038/334248a0. Nature. 1988. PMID: 2899844

4

Exclusion of the Friedreich ataxia gene from chromosome 19.

Chamberlain S, Worrall CS, South S, Shaw J, Farrall M, Williamson R. Chamberlain S, et al. Among authors: farrall m. Hum Genet. 1987 Jun;76(2):186-90. doi: 10.1007/BF00284919. Hum Genet. 1987. PMID: 3475247

5

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: farrall m. Am J Hum Genet. 1993 Jan;52(1):99-109. Am J Hum Genet. 1993. PMID: 8434613 Free PMC article.

6

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.

Auburger G, Diaz GO, Capote RF, Sanchez SG, Perez MP, del Cueto ME, Meneses MG, Farrall M, Williamson R, Chamberlain S, et al. Auburger G, et al. Among authors: farrall m. Am J Hum Genet. 1990 Jun;46(6):1163-77. Am J Hum Genet. 1990. PMID: 1971152 Free PMC article.

7

Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus.

Twells R, Yenchitsomanus PT, Sirinavin C, Allotey R, Poungvarin N, Viriyavejakul A, Cemal C, Weber J, Farrall M, Rodprasert P, et al. Twells R, et al. Among authors: farrall m. Hum Mol Genet. 1994 Jan;3(1):177-80. doi: 10.1093/hmg/3.1.177. Hum Mol Genet. 1994. PMID: 8162021

8

Isolation of a polymorphic genomic clone from chromosome 7. Physical and genetic linkage studies to markers around the cystic fibrosis locus.

Davies KA, Lorand L, Waterfield M, Wainwright B, Farrall M, Williamson R. Davies KA, et al. Among authors: farrall m. Hum Genet. 1987 Oct;77(2):122-6. doi: 10.1007/BF00272377. Hum Genet. 1987. PMID: 2888718

9

The gene CYP3 encoding P450pcn1 (nifedipine oxidase) is tightly linked to the gene COL1A2 encoding collagen type 1 alpha on 7q21-q22.1.

Brooks BA, McBride OW, Dolphin CT, Farrall M, Scambler PJ, Gonzalez FJ, Idle JR. Brooks BA, et al. Among authors: farrall m. Am J Hum Genet. 1988 Sep;43(3):280-4. Am J Hum Genet. 1988. PMID: 2901225 Free PMC article.

10

Chorea-acanthocytosis: genetic linkage to chromosome 9q21.

Rubio JP, Danek A, Stone C, Chalmers R, Wood N, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Manfredi M, Vance J, Pericak-Vance M, Brown R, Rudolf G, Picard F, Alonso E, Brin M, Németh AH, Farrall M, Monaco AP. Rubio JP, et al. Among authors: farrall m. Am J Hum Genet. 1997 Oct;61(4):899-908. doi: 10.1086/514876. Am J Hum Genet. 1997. PMID: 9382101 Free PMC article.

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