Authors: Alitalo, Tuina Kruse, Torben A. Forsius, Henrik Eriksson, Aldur W. de la Chapelle, Albert

Citation: Alitalo, Tuina et al., Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis., American journal of human genetics , 48-I(1), 1991, pp. 31-38

Authors: Levinson, Barbara Lehesjoki, Anna-Elina de la Chapelle, Albert Gitschier, Jane

Citation: Levinson, Barbara et al., Molecular analysis of hemophilia A mutations in the finnish population, American journal of human genetics , 46-I(1), 1990, pp. 53-62

Authors: Sims, Katherine B. Ozelius, Laurie Corey, Timothy Rinehart, William B. Liberfarb, Ruth Haines, Jonathan Chen, Wei lane Norio, Reijo Sankila, Eeva de la Chapelle, Albert Murphy, Dennis L. Gusella, James Breakefield, Xandra O.

Citation: B. Sims, Katherine et al., Norrie disease gene Is distinct from the monoamine oxidase genes, American journal of human genetics , 45-I(3), 1989, pp. 424-434

Authors: Lindlöf, Mikael Anne Kiuru, Kääriäinen, Helena Kalimo, Hannu Lang, Heikki Pihko, Helena Rapola, Juhani Somer, Hannu Somer, Mirja Savontaus, Marja-Lisa de la Chapelle, Albert

Citation: Lindlöf, Mikael et al., Gene deletions in X-linked muscular dystrophy, American journal of human genetics , 44(4), 1989, pp. 496-503

Authors: Wagner, Anja Barrows, Alicia Wijnen, Juul Th. Klift, Heleen, Van : der Franken, Patrick F. Verkuijlen, Paul Nakagawa, Hidewaki Geugien, Marjan Jaghmohan-Changur, Shantie Breukel, Cor Meijers-Hijboer, Hanne Morreau, Hans Puijenbroek, Marjo, Van Burn, John Coronel, Stephany Kinarski, Yulia Okimoto, Ross Watson, Patrice Lynch, Jane F. de la Chapelle, Albert Lynch, Henry T. Fodde, Riccardo

Citation: Wagner, Anja et al., Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an American Founder Genomic Deletion of the MSH2 Gene, American journal of human genetics , 72(5), 2003, pp. 1088-1100

Authors: Kolehmainen, Juha Black, Graeme C.M. Saarinen, Anne Chandler, Kate Clayton-Smith, Jill Träskelin, Ann-Liz Perveen, Rahat Kivitie-Kallio, Satu Norio, Reijo Warburg, Mette Fryns, Jean-Pierre de la Chapelle, Albert Lehesjoki, Anna-Elina

Citation: Kolehmainen, Juha et al., Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport, American journal of human genetics , 72(6), 2003, pp. 1359-1369