Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2 von Jakobs, Petra M., Hess, John F., FitzGerald, Paul G., Kramer, Patricia, Weleber, Richard G., Litt, Michael

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Fifty-Four New Gene-Based Canine Microsatellite Markers von Litt, M, Bestwick, M. L, Winther, M. J, Jakobs, P. M

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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p von Whitney, Michael, Thayer, Matt, Reifsteck, Carol, Olson, Susan, Smith, Leslie, Jakobs, Petra M., Leach, Robin, Naylor, Susan, Joenje, Hans, Grompe, Markus

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Mammalian SNM1 is required for genome stability von Hemphill, A.W., Bruun, D., Thrun, L., Akkari, Y., Torimaru, Y., Hejna, K., Jakobs, P.M., Hejna, J., Jones, S., Olson, S.B., Moses, R.E.

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Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3 von Hejna, James A., Timmers, Cynthia D., Reifsteck, Carol, Bruun, Donald A., Lucas, Lora W., Jakobs, Petra M., Toth-Fejel, SuEllen, Unsworth, Nancy, Clemens, Susan L., Garcia, Dawn K., Naylor, Susan L., Thayer, Mathew J., Olson, Susan B., Grompe, Markus, Moses, Robb E.

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Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease von Jakobs, Petra M., Hanson, Emily L., Crispell, Kathy A., Toy, Warren, Keegan, Hugh, Schilling, Karla, Icenogle, Timothy B., Litt, Michael, Hershberger, Ray E.

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Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure von Li, Duanxiang, Parks, Sharie B., Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Partain, Julie, Nixon, Randal R., Allen, Charles N., Irwin, Robert P., Jakobs, Petra M., Litt, Michael, Hershberger, Ray E.

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Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases von Hejna, James A., Saito, Hiroshi, Merkens, Louise S., Tittle, Thomas V., Jakobs, Petra M., Whitney, Michael A., Grompe, Markus, Friedberg, Andrew S., Moses, Robb E.

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews von Whitney, Michael A., Saito, Hiroshi, Jakobs, Petra M., Gibson, Rachel A., Moses, Robb E., Grompe, Markus

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Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure von Jakobs, P M, Sahaayaruban, P, Saito, H, Reifsteck, C, Olson, S, Joenje, H, Moses, R E, Grompe, M

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Complementation group assignments in Fanconi anemia fibroblast cell lines from North America von Jakobs, P M, Fiddler-Odell, E, Reifsteck, C, Olson, S, Moses, R E, Grompe, M

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Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome von Jakobs, P M, Smith, L, Thayer, M, Grompe, M

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Topo IIIα and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents von Hemphill, A.W., Akkari, Y., Newell, A.H., Schultz, R.A., Grompe, M., North, P.S., Hickson, I.D., Jakobs, P.M., Rennie, S., Pauw, D., Hejna, J., Olson, S.B., Moses, R.E.

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Monoaminergic-peptidergic interactions in neuroregulatory control of the cephalic aorta in Sepia officinalis L. (cephalopoda) von Schipp, R., Jakobs, P.M., Fiedler, A.

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The electrocardiogram of Sepia officinalis L. (cephalopoda: coleoida) and its modulation by neuropeptides of the FMRFamide group von Jakobs, P.M., Schipp, R.

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Topo III[alpha] and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents von Hemphill, A W, Akkari, Y, Newell, A H, Schultz, R A, Grompe, M, North, P S, Hickson, I D, Jakobs, P M, Rennie, S, Pauw, D, Hejna, J, Olson, S B, Moses, R E

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Topo IIIa and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents von Hemphill, A W, Akkari, Y, Newell, AH, Schultz, R A, Grompe, M, North, P S, Hickson, I D, Jakobs, P M, Rennie, S, Pauw, D, Hejna, J, Olson, S B, Moses, R E

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A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation von Hershberger, Ray E., Hanson, Emily L., Jakobs, Petra M., Keegan, Hugh, Coates, Kelly, Bousman, Sylvia, Litt, Michael

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Fanconi anemia cells have a normal gene structure for topoisomerase I von Saito, H, Grompe, M, Neeley, T L, Jakobs, P M, Moses, R E

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Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia von Lensch, M. William, Tischkowitz, Marc, Christianson, Tracy A., Reifsteck, Carol A., Speckhart, S. Ashley, Jakobs, Petra M., O’Dwyer, Michael E., Olson, Susan B., Le Beau, Michelle M., Hodgson, Shirley V., Mathew, Christopher G., Larson, Richard A., Bagby, Grover C.

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