Menkes and Wilson diseases. by Monaco, A, Chelly, J

Cloning the Wilson disease gene. by Chelly, J, Monaco, A

Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach. by Fairweather, N, Chelly, J, Monaco, A

Isolation of DNTR polymorphisms from yeast artificial chromosomes encompassing X chromosomal loci PGK1 and DXS56. by Graeber, M, Monaco, A, Chelly, J, Müller, U

DXS106 AND DXS559 FLANK THE X-LINKED DYSTONIA-PARKINSONISM LOCUS, DYT3 by Wagner, T, Fairweather, N, Chelly, J, Monaco, A, Muller, U

DIVERSITY OF THE DYSTROPHIN GENE-PRODUCTS by Chelly, J, Hugnot, J, Monaco, A, Kaplan, J, Kahn, A

YAC CONTIGS IN XQ12-]Q13.1 by Rider, S, Fairweather, N, Chelly, J, Wagner, T, Muller, U, Monaco, A

A Golgi localization signal identified in the Menkes recombinant protein. by Francis, M, Jones, E, Levy, E, Ponnambalam, S, Chelly, J, Monaco, A

PHYSICAL AND GENETIC-MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XCEN-]Q21 by Chelly, J, Rider, S, Fairweather, N, Ishikawabrush, Y, Muscatelli, F, Monaco, A

Characterization of the exon structure of the Menkes disease gene using vectorette PCR. by Tümer, Z, Vural, B, Tønnesen, T, Chelly, J, Monaco, A, Horn, N

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3). by Müller, U, Haberhausen, G, Wagner, T, Fairweather, N, Chelly, J, Monaco, A

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. by Ho, M, Chelly, J, Carter, N, Danek, A, Crocker, P, Monaco, A

XIST IS NOT REQUIRED FOR THE MAINTENANCE OF X-INACTIVATION - ANALYSIS OF THE X-CHROMOSOME BREAKPOINT REGION AT XQ13 IN PATIENTS WITH ACQUIRED ISODICENTRIC X-CHROMOSOME ASSOCIATED W... by Rider, S, Rack, K, Chelly, J, Lafreniere, R, Willard, H, Buckle, V, Monaco, A

PHYSICAL MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XP21 by Walker, A, Ho, M, Muscatelli, F, Chelly, J, Clarke, E, Ishikawabrush, Y, Monaco, A

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

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) by Fairweather, N, Bell, C, Cochrane, S, Chelly, J, Wang, S, Mostacciuolo, M, Monaco, A, Haites, N

A 2.6-MB YAC CONTIG OF THE HUMAN X-INACTIVATION CENTER REGION IN XQ13 - PHYSICAL LINKAGE OF THE RPS4X, PHKA1, XIST, AND DXS128E GENES AND REFINEMENT OF THE XIC-CONTAINING INTERVAL by Lafreniere, R, Brown, C, Rider, S, Chelly, J, Taillonmiller, P, Chinault, C, Monaco, A, Willard, H

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes. by Lafrenière, R, Brown, C, Rider, S, Chelly, J, Taillon-Miller, P, Chinault, A, Monaco, A, Willard, H

Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice. by George, A, Reed, V, Glenister, P, Chelly, J, Tümer, Z, Horn, N, Monaco, A, Boyd, Y

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