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Nature Genetics|May 1, 1995
Mutations associated with familial melanoma impair p16INK4 functionK Ranade, C J Hussussian, R S Sikorski, et al.Nature Genetics|May 1, 1995
Loss of function effect of RET mutations causing Hirschsprung diseaseB Pasini, M G Borrello, A Greco, et al.Nature Genetics|May 1, 1995
Comparative sequence analysis of the human and pufferfish Huntington's disease genesS Baxendale, S Abdulla, G Elgar, et al.Nature Genetics|May 1, 1995
Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brainI Yazawa, N Nukina, H Hashida, et al.Nature Genetics|June 1, 1995
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domainsJ Hughes, C J Ward, B Peral, et al.Nature Genetics|June 1, 1995
A novel gene, Translin, encodes a recombination hotspot binding protein associated with chromosomal translocationsK Aoki, K Suzuki, T Sugano, et al.Nature Genetics|June 1, 1995
Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1L E Figuera, M Pandolfo, P W Dunne, et al.Nature Genetics|April 1, 1993
The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTRC Li, M Ramjeesingh, E Reyes, et al.Nature Genetics|April 1, 1993
A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplexA Hovnanian, E Pollack, L Hilal, et al.Pageof 745