Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease I. Kanazawa Review Article Pages: 1 - 17
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis Kamel Ben OthmaneJulie M. RochelleJ. M. Vance Original article Pages: 18 - 23
HLA typing in the United Kingdom multiple sclerosis genome screen Francesca CoradduStephen SawcerA. Compston Original Article Pages: 24 - 33
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33 Betsy A. HoslerPeter C. SappC. B. Day Original article Pages: 34 - 42
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis Christina FuchsThomas LiehrB. Rautenstrauss Original article Pages: 43 - 46
Mapping, genomic structure, and polymorphisms of the human GABA B R1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy Howard Christian PetersGudrun KämmerO. Riess Original article Pages: 47 - 54
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers Afif HentatiKarim OuahchiT. Siddique Original article Pages: 55 - 60
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission Catherine BessouJean-Bernard GiugiaL. Ségalat Original article Pages: 61 - 72
The NF2 gene and merlin protein in human osteosarcomas A. O. Stemmer-RachamimovG. P. NielsenL. B. Jacoby Letter to the editor Pages: 73 - 74
Transcript map of the chromosome 2-linked autosomal dominant spastic paraplegia (SPG4) critical region and identification of a highly informative STRP En-Lieng LauMarkus KostrzewaUlrich Müller Letter to the editor Pages: 75 - 76
