Hästbacka J, Kerrebrock A, Mokkala K, et al. Identification of the Finnish founder mutation for diastrophic dysplasia (DTD). Eur J Hum Genet. 1999;7(6):664-70. doi:10.1038/sj.ejhg.5200361
McCarthy MI, Kruglyak L, Lander ES. Sib-pair collection strategies for complex diseases. Genet Epidemiol. 1998;15(4):317-40. doi:10.1002/(SICI)1098-2272(1998)15:4<317::AID-GEPI1>3.0.CO;2-#
Batzoglou S, Berger B, Mesirov J, Lander ES. Sequencing a genome by walking with clone-end sequences: a mathematical analysis. Genome Res. 1999;9(12):1163-74.
Lincoln SE, Lander ES. Systematic detection of errors in genetic linkage data. Genomics. 1992;14(3):604-10.
Klockars T, Holmberg V, Savukoski M, Lander ES, Peltonen L. Transcript identification on the CLN5 region on chromosome 13q22. Hum Genet. 1999;105(1-2):51-6.
Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nat Genet. 1992;2(3):204-11. doi:10.1038/ng1192-204
Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11(3):241-7. doi:10.1038/ng1195-241
Hacia JG, Fan JB, Ryder O, et al. Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays. Nat Genet. 1999;22(2):164-7. doi:10.1038/9674
Van Etten WJ, Steen RG, Nguyen H, et al. Radiation hybrid map of the mouse genome. Nat Genet. 1999;22(4):384-7. doi:10.1038/11962
Nusbaum C, Slonim DK, Harris KL, et al. A YAC-based physical map of the mouse genome. Nat Genet. 1999;22(4):388-93. doi:10.1038/11967