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Page 1
An STS-based map of the human genome.
Hudson TJ, Stein LD, Gerety SS, Ma J, Castle AB, Silva J, Slonim DK, Baptista R, Kruglyak L, Xu SH, Hu X, Colbert AM, Rosenberg C, Reeve-Daly MP, Rozen S, Hui L, Wu X, Vestergaard C, Wilson KM, Bae JS, Maitra S, Ganiatsas S, Evans CA, DeAngelis MM, Ingalls KA, Nahf RW, Horton LT Jr, Anderson MO, Collymore AJ, Ye W, Kouyoumjian V, Zemsteva IS, Tam J, Devine R, Courtney DF, Renaud MT, Nguyen H, O'Connor TJ, Fizames C, Fauré S, Gyapay G, Dib C, Morissette J, Orlin JB, Birren BW, Goodman N, Weissenbach J, Hawkins TL, Foote S, Page DC, Lander ES. Hudson TJ, et al. Science. 1995 Dec 22;270(5244):1945-54. doi: 10.1126/science.270.5244.1945. Science. 1995. PMID: 8533086
Sib-pair collection strategies for complex diseases.
McCarthy MI, Kruglyak L, Lander ES. McCarthy MI, et al. Genet Epidemiol. 1998;15(4):317-40. doi: 10.1002/(SICI)1098-2272(1998)15:4<317::AID-GEPI1>3.0.CO;2-#. Genet Epidemiol. 1998. PMID: 9671984
A locus for Fanconi anemia on 16q determined by homozygosity mapping.
Gschwend M, Levran O, Kruglyak L, Ranade K, Verlander PC, Shen S, Faure S, Weissenbach J, Altay C, Lander ES, Auerbach AD, Botstein D. Gschwend M, et al. Am J Hum Genet. 1996 Aug;59(2):377-84. Am J Hum Genet. 1996. PMID: 8755924 Free PMC article.