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Nature Genetics|September 1, 1994
p53-deficient mice are extremely susceptible to radiation-induced tumorigenesisC J Kemp, T Wheldon, A BalmainNature Genetics|September 1, 1994
A radiation hybrid map of 506 STS markers spanning human chromosome 11M R James, C W Richard, J J Schott, et al.Nature Genetics|September 1, 1994
Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4M H Polymeropoulos, R G Swift, M SwiftNature Genetics|September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeW Reardon, R M Winter, P Rutland, et al.Nature Genetics|August 1, 1994
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversalB Bardoni, E Zanaria, S Guioli, et al.Nature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.Nature Genetics|August 1, 1994
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American familyJ R Burke, M S Wingfield, K E Lewis, et al.Nature Genetics|June 1, 1994
Association between atopy and variants of the beta subunit of the high-affinity immunoglobulin E receptorT Shirakawa, A Li, M Dubowitz, et al.Nature Genetics|June 1, 1994
A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouseS G Ryan, M S Buckwalter, J W Lynch, et al.Nature Genetics|June 1, 1994
Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan geneH Watanabe, K Kimata, S Line, et al.Pageof 744