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Nature Genetics|October 25, 2011
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosisYohei Takahashi, Ikuyo Kou, Atsushi Takahashi, et al.Nature Genetics|October 25, 2011
A rare penetrant mutation in CFH confers high risk of age-related macular degenerationSoumya Raychaudhuri, Oleg Iartchouk, Kimberly Chin, et al.Nature Genetics|October 25, 2011
Natural variation in GS5 plays an important role in regulating grain size and yield in riceYibo Li, Chuchuan Fan, Yongzhong Xing, et al.Nature Genetics|March 1, 1996
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeG Pilia, R M Hughes-Benzie, A MacKenzie, et al.Nature Genetics|March 1, 1996
Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophyA Nagano, R Koga, M Ogawa, et al.Nature Genetics|March 1, 1996
A human chondrodysplasia due to a mutation in a TGF-beta superfamily memberJ T Thomas, K Lin, M Nandedkar, et al.Nature Genetics|March 1, 1996
Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient miceE Hummler, P Barker, J Gatzy, et al.Nature Genetics|February 1, 1996
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemiaT Nakamura, D A Largaespada, M P Lee, et al.Nature Genetics|February 1, 1996
Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyriaR L Lindberg, C Porcher, B Grandchamp, et al.Nature Genetics|February 1, 1996
Differential regulation of telomerase activity and telomerase RNA during multi-stage tumorigenesisM A Blasco, M Rizen, C W Greider, et al.Pageof 745