ORA - Oxford University Research Archive

1 - 7 of 7

1

Journal article

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

Lloyd, SE, Gunther, W, Pearce, SH, et al.
1997-08-05

2

Journal article

Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.

Fisher, SE, Ciccodicola, A, Tanaka, K, et al.
1997-10-05

3

Journal article

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.

Fisher, SE, Marlow, AJ, Lamb, J, et al.
1999-01-05

4

Journal article

A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).

Fisher, SE, Stein, JF, Monaco, AP
1999-01-01

5

Conference

Localisation of a gene implicated in a severe speech and language disorder.

Fisher, SE, Vargha-Khadem, F, Watkins, K, et al.
1997-10-05

6

Journal article

Localisation of a gene implicated in a severe speech and language disorder.

Fisher, SE, Vargha-Khadem, F, Watkins, KE, et al.
1998-02-05

7

Journal article

Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis.

Tanaka, K, Fisher, SE, Craig, IW
1999-06-05

TO TOP