Positional cloning of an X;8 translocation (p22.13;q22.1) associated with multiple exostoses and autism av Ishikawa-Brush, Y

Fluorescence in situ hybridisation of multiple probes on a single microscope slide. av Larin, Z, Fricker, M, Maher, E, Ishikawa-Brush, Y, Southern, E

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease. av Tümer, Z, Chelly, J, Tommerup, N, Ishikawa-Brush, Y, Tønnesen, T, Monaco, A, Horn, N

Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1). av Bolton, P, Powell, J, Rutter, M, Buckle, V, Yates, JR, Ishikawa-Brush, Y, Monaco, A

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. av Chelly, J, Tümer, Z, Tønnesen, T, Petterson, A, Ishikawa-Brush, Y, Tommerup, N, Horn, N, Monaco, A

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. av Ishikawa-Brush, Y, Powell, J, Bolton, P, Miller, A, Francis, F, Willard, H, Lehrach, H, Monaco, A

Construction of a YAC contig spanning the Xq13.3 subband. av Villard, L, Gecz, J, Colleaux, L, Lossi, A, Chelly, J, Ishikawa-Brush, Y, Monaco, A, Fontes, M

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes. av Walker, A, Chelly, J, Love, DR, Brush, Y, Récan, D, Chaussain, J, Oley, C, Connor, J, Yates, J, Price, D

Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines. av Francis, F, Benham, F, See, C, Fox, M, Ishikawa-Brush, Y, Monaco, A, Weiss, B, Rappold, G, Hamvas, R, Lehrach, H

A genome-wide screen for quantitative trait loci involved in developmental dyslexia in a large sample of sib-pairs from the UK av Francks, C, Fisher, S, Marlow, A, Williams, D, Ishikawa-Brush, Y, Talcott, J, Weeks, D, Cardon, L, Richardson, A, Stein, J, Monaco, A

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions. av Huber, I, Bitner-Glindzicz, M, de Kok, Y, van der Maarel, S, Ishikawa-Brush, Y, Monaco, A, Robinson, D, Malcolm, S, Pembrey, M, Brunner, H

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. av Fisher, S, Francks, C, Marlow, A, MacPhie, I, Newbury, D, Cardon, L, Ishikawa-Brush, Y, Richardson, A, Talcott, J, Gayán, J, Olson, R, Pennington, B, Smith, S, DeFries, J, Stein, J, Monaco, A

Quantitative trait analysis of the entire genome in large samples of dyslexic sib-pairs from the UK and US. av Fisher, S, Francks, C, Marlow, A, MacPhie, I, Newbury, D, Cardon, L, Ishikawa-Brush, Y, Richardson, A, Talcott, J, Gayan, J, Olson, R, Pennington, B, Smith, S, DeFries, J, Stein, J, Monaco, A