Authors:
Shiloh, Yosef
Litvak, Gilad
Ziv, Yael
Lehner, Thomas
SAndkuyl, Lodewijk
Hidesheimen, Minka
Buchris, Vered
Cremes, Frans P.M.
Szabo, Paul
White, Bradley N.
Holden, Janette J. A.
Ott, Jurg
Citation: Shiloh, Yosef et al., Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.1, American journal of human genetics , 47-I(1), 1990, pp. 20-27
Authors:
Ellison, KimberlyA.
Fill, CarolynP.
Terwilliger, Joseph
DeGennaro, LouisJ.
Martin-Gallardo, Antonia
Anvret, Maria
Percy, AlanK.
Ott, Jurg
Zoghbi, Huda
Citation: Ellison, Kimberlya et al., Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis., American journal of human genetics , 50-I(2), 1992, pp. 278-287
Authors:
Martinez-Mir, Amalia
Zlotogorski, Abraham
Gordon, Derek
Petukhova, Lynn
Mo, Jianhong
Gilliam, T. Conrad
Londono, Douglas
Haynes, Chad
Ott, Jurg
Hordinsky, Maria
Nanova, Krassimira
Norris, David
Prince, Vera
Duvic, Madeleine
Christiano, Angela M.
Citation: Martinez-mir, Amalia et al., Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata, American journal of human genetics , 80(2), 2007, pp. 316-328
Authors:
Vilkki, Johanna
Ott, Jurg
Savontaus, Marja-Lissa
Aula, Pertti
Nikoskelainen, Eeva K.
Citation: Vilkki, Johanna et al., Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7., American journal of human genetics , 48-I(3), 1991, pp. 486-491
Authors:
Mérette, Chantal
King, Mary-Claire
Ott, Jurg
Citation: Mérette, Chantal et al., Heterogeneity analysis of breast cancer families by using age at onset as a covariate., American journal of human genetics , 50-I(3), 1992, pp. 515-519
Authors:
Majewski, Jacek
Schultz, Dennis W.
Welber, Richard G.
Schain, Mitchell B.
Edwards, Albert O.
Matise, Tara C.
Acott, Ted S.
Ott, Jurg
Klein, Michael L.
Citation: Majewski, Jacek et al., Age-Related Macular Degeneration.a Genome Scan in Extended Families, American journal of human genetics , 73(3), 2003, pp. 540-550