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Nature Genetics|November 5, 1997
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophyS M Gu, D A Thompson, C R Srikumari, et al.Nature Genetics|November 5, 1997
Increased stress response and beta-phenylethylamine in MAOB-deficient miceJ Grimsby, M Toth, K Chen, et al.Nature Genetics|November 5, 1997
Telomeric localization of TRF2, a novel human telobox proteinT Bilaud, C Brun, K Ancelin, et al.Nature Genetics|November 5, 1997
Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndromeJ A McGrath, J R McMillan, C S Shemanko, et al.Nature Genetics|February 14, 1998
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretchS Igarashi, R Koide, T Shimohata, et al.Nature Genetics|February 14, 1998
Distinct interactions of PML-RARalpha and PLZF-RARalpha with co-repressors determine differential responses to RA in APLL Z He, F Guidez, C Tribioli, et al.Nature Genetics|February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiencyW Wu, J D Cogan, R W Pfäffle, et al.Nature Genetics|February 14, 1998
Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregatesD Martindale, A Hackam, A Wieczorek, et al.Nature Genetics|February 14, 1998
Evolutionary sequence comparisons using high-density oligonucleotide arraysJ G Hacia, W Makalowski, K Edgemon, et al.Pageof 745