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Nature Genetics|March 18, 1999
Genomic profiling of drug sensitivities via induced haploinsufficiencyG Giaever, D D Shoemaker, T W Jones, et al.Nature Genetics|March 18, 1999
Notch signalling pathway mediates hair cell development in mammalian cochleaP J Lanford, Y Lan, R Jiang, et al.Nature Genetics|March 18, 1999
SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intoleranceG Borsani, M T Bassi, M P Sperandeo, et al.Nature Genetics|March 18, 1999
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1M Aminoff, J E Carter, R B Chadwick, et al.Nature Genetics|January 31, 2006
Dominance relationships between self-incompatibility alleles controlled by DNA methylationHiroshi Shiba, Tomohiro Kakizaki, Megumi Iwano, et al.Nature Genetics|January 31, 2006
A SNP in the ABCC11 gene is the determinant of human earwax typeKoh-ichiro Yoshiura, Akira Kinoshita, Takafumi Ishida, et al.Nature Genetics|February 14, 2006
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndromeTetsuya Niihori, Yoko Aoki, Yoko Narumi, et al.Nature Genetics|January 18, 2006
Evolution of new protein topologies through multistep gene rearrangementsSergio G Peisajovich, Liat Rockah, Dan S TawfikNature Genetics|January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk ratUrsula M Smith, Mark Consugar, Louise J Tee, et al.Nature Genetics|December 18, 2007
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosisMichael A van Es, Paul W J van Vught, Hylke M Blauw, et al.Pageof 745