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Nature Genetics|September 1, 1993
Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1BT Kulkens, P A Bolhuis, R A Wolterman, et al.Nature Genetics|November 1, 1993
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia AD Lakich, H H Kazazian, S E Antonarakis, et al.Nature Genetics|July 1, 1995
Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate geneM L Budarf, J Collins, W Gong, et al.Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.Nature Genetics|July 1, 1995
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseS Fuchs, M Nakazawa, M Maw, et al.Nature Genetics|August 1, 1995
New HLA-DPB1 alleles generated by interallelic gene conversion detected by analysis of spermG Zangenberg, M M Huang, N Arnheim, et al.Nature Genetics|August 1, 1995
Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumoursE F Schoenmakers, S Wanschura, R Mols, et al.Nature Genetics|August 1, 1995
Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'D L Burgess, D C Kohrman, J Galt, et al.Nature Genetics|April 1, 1995
Lung disease in the cystic fibrosis mouse exposed to bacterial pathogensD J Davidson, J R Dorin, G McLachlan, et al.Pageof 742