1.
Superti-Furga A, Hästbacka J, Rossi A, et al. A family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans. Ann N Y Acad Sci. 1996;785:195-201.
Eric Lander
1.
Kurooka H, Segre JA, Hirano Y, et al. Rescue of the hairless phenotype in nude mice by transgenic insertion of the wild-type Hfh11 genomic locus. Int Immunol. 1996;8(6):961-6.
1.
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet. 1996;58(6):1347-63.
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Kruglyak L, Lander ES. Limits on fine mapping of complex traits. Am J Hum Genet. 1996;58(5):1092-3.
1.
Dietrich WF, Miller J, Steen R, et al. A comprehensive genetic map of the mouse genome. Nature. 1996;380(6570):149-52. doi:10.1038/380149a0.
1.
Hamilton BA, Frankel WN, Kerrebrock AW, et al. Disruption of the nuclear hormone receptor RORalpha in staggerer mice. Nature. 1996;379(6567):736-9. doi:10.1038/379736a0.
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Hästbacka J, Superti-Furga A, Wilcox WR, Rimoin DL, Cohn DH, Lander ES. Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias. Am J Hum Genet. 1996;58(2):255-62.
1.
Yi TM, Lander ES. Iterative template refinement: protein-fold prediction using iterative search and hybrid sequence/structure templates. Methods Enzymol. 1996;266:322-39.
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Galli J, Li LS, Glaser A, et al. Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat. Nat Genet. 1996;12(1):31-7. doi:10.1038/ng0196-31.
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Brown DM, Provoost AP, Daly MJ, Lander ES, Jacob HJ. Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat. Nat Genet. 1996;12(1):44-51. doi:10.1038/ng0196-44.