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Nature Genetics|August 1, 1997
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrixH Winter, M A Rogers, L Langbein, et al.Nature Genetics|June 1, 1997
A new dimension for the human genome project: towards comprehensive expression mapsT Strachan, M Abitbol, D Davidson, et al.Nature Genetics|June 1, 1997
The BCL-6 proto-oncogene controls germinal-centre formation and Th2-type inflammationB H Ye, G Cattoretti, Q Shen, et al.Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.Nature Genetics|June 1, 1997
Localization of genes controlling resistance to trypanosomiasis in miceS J Kemp, F Iraqi, A Darvasi, et al.Nature Genetics|June 1, 1997
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21T A Mansfield, D B Simon, Z Farfel, et al.Nature Genetics|December 13, 2005
Dosage compensation of the active X chromosome in mammalsDi Kim Nguyen, Christine M DistecheNature Genetics|December 13, 2005
Defective planar cell polarity in polycystic kidney diseaseEvelyne Fischer, Emilie Legue, Antonia Doyen, et al.Nature Genetics|November 10, 2009
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis riskSoumya Raychaudhuri, Brian P Thomson, Elaine F Remmers, et al.Nature Genetics|November 10, 2009
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapyColin J D Ross, Hagit Katzov-Eckert, Marie-Pierre Dubé, et al.Pageof 743