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
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