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Nature Genetics|July 10, 2012
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysmMark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, et al.Nature Genetics|August 19, 2020
Extrachromosomal DNA is associated with oncogene amplification and poor outcome across multiple cancersHoon Kim, Nam-Phuong Nguyen, Kristen Turner, et al.Nature Genetics|August 11, 1998
Positional cloning of the gene for X-linked retinitis pigmentosa 2U Schwahn, S Lenzner, J Dong, et al.Nature Genetics|August 11, 1998
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethalityS Hirotsune, M W Fleck, M J Gambello, et al.Nature Genetics|August 11, 1998
Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4V Korinek, N Barker, P Moerer, et al.Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.Nature Genetics|September 10, 1998
Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiencyJ Reiss, N Cohen, C Dorche, et al.Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.Nature Genetics|July 14, 1998
Role of the region 3' to Xist exon 6 in the counting process of X-chromosome inactivationP Clerc, P AvnerNature Genetics|July 14, 1998
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.Pageof 745