Authors: Jakobs, PM Hanson, EL Crispell, KA Toy, W Keegan, H Schilling, K Icenogle, TB Litt, M Hershberger, RE

Citation: Pm. Jakobs et al., Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease, J CARD FAIL, 7(3), 2001, pp. 249-256

Authors: Hejna, JA Timmers, CD Reifsteck, C Bruun, DA Lucas, LW Jakobs, PM Toth-Fejel, S Unsworth, N Clemens, SL Garcia, DK Naylor, SL Thayer, MJ Olson, SB Grompe, M Moses, RE

Citation: Ja. Hejna et al., Localization of the fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3, AM J HU GEN, 66(5), 2000, pp. 1540-1551

Authors: Jakobs, PM Hess, JF FitzGerald, PG Kramer, P Weleber, RG Litt, M

Citation: Pm. Jakobs et al., Autosomal-dominant congenital cataract associated with a deletion mutationin the human beaded filament protein gene BFSP2, AM J HU GEN, 66(4), 2000, pp. 1432-1436

Authors: Jakobs, PM Smith, L Thayer, M Grompe, M

Citation: Pm. Jakobs et al., Embryonic stem cells can be used to construct hybrid cell lines containinga single, selectable murine chromosome, MAMM GENOME, 10(4), 1999, pp. 381-384