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Nature Genetics|May 12, 2015
The impact of low-frequency and rare variants on lipid levelsIda Surakka, Momoko Horikoshi, Reedik Mägi, et al.
Nature Genetics|May 5, 2015
Mapping long-range promoter contacts in human cells with high-resolution capture Hi-CBorbala Mifsud, Filipe Tavares-Cadete, Alice N Young, et al.
Nature Genetics|May 5, 2015
A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancerRobbert D A Weren, Marjolijn J L Ligtenberg, C Marleen Kets, et al.
Nature Genetics|January 13, 1998
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinaseD E Jenne, H Reimann, J Nezu, et al.
Nature Genetics|January 13, 1998
An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemiaA Wiestner, R J Schlemper, A P van der Maas, et al.
Nature Genetics|January 13, 1998
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse modelE M Southard-Smith, L Kos, W J Pavan
Nature Genetics|January 13, 1998
A polymorphism in the regulatory region of APOE associated with risk for Alzheimer's dementiaM J Bullido, M J Artiga, M Recuero, et al.
Nature Genetics|January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNAM D Koob, K A Benzow, T D Bird, et al.
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