Farrall M - Search Results

1

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.

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

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

4

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

5

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.

6

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

7

Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions.

Dixon MJ, Haan E, Baker E, David D, McKenzie N, Williamson R, Mulley J, Farrall M, Callen D. Dixon MJ, et al. Among authors: farrall m. Am J Hum Genet. 1991 Feb;48(2):274-80. Am J Hum Genet. 1991. PMID: 1671319 Free PMC article.

8

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.

9

Predisposing locus for Alzheimer's disease on chromosome 21.

Goate AM, Haynes AR, Owen MJ, Farrall M, James LA, Lai LY, Mullan MJ, Roques P, Rossor MN, Williamson R, et al. Goate AM, et al. Among authors: farrall m. Lancet. 1989 Feb 18;1(8634):352-5. doi: 10.1016/s0140-6736(89)91725-x. Lancet. 1989. PMID: 2563508

10

Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study.

Estivill X, Farrall M, Williamson R, Ferrari M, Seia M, Giunta AM, Novelli G, Potenza L, Dallapicolla B, Borgo G, et al. Estivill X, et al. Among authors: farrall m. Am J Hum Genet. 1988 Jul;43(1):23-8. Am J Hum Genet. 1988. PMID: 2897786 Free PMC article.

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