Hildegard Kehrer-Sawatzki
Abteilung Humangenetik
Universität Ulm
Albert-Einstein-Allee 11
89081
Germany
Name/email consistency: high
- Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans. Kehrer-Sawatzki, H., Sandig, C.A., Goidts, V., Hameister, H. Cytogenet. Genome Res. (2005)
- Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes). Kehrer-Sawatzki, H., Sandig, C., Chuzhanova, N., Goidts, V., Szamalek, J.M., Tänzer, S., Müller, S., Platzer, M., Cooper, D.N., Hameister, H. Hum. Mutat. (2005)
- Extensively high load of internal tumors determined by whole body MRI scanning in a patient with neurofibromatosis type 1 and a non-LCR-mediated 2-Mb deletion in 17q11.2. Kehrer-Sawatzki, H., Kluwe, L., Fünsterer, C., Mautner, V.F. Hum. Genet. (2005)
- Molecular characterization of the pericentric inversion of chimpanzee chromosome 11 homologous to human chromosome 9. Kehrer-Sawatzki, H., Szamalek, J.M., Tänzer, S., Platzer, M., Hameister, H. Genomics (2005)
- Interstitial deletion del(10)(q25.2q25.3 approximately 26.11)--case report and review of the literature. Kehrer-Sawatzki, H., Daumiller, E., Müller-Navia, J., Kendziorra, H., Rossier, E., du Bois, G., Barbi, G. Prenat. Diagn. (2005)
- High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 gene. Kehrer-Sawatzki, H., Kluwe, L., Sandig, C., Kohn, M., Wimmer, K., Krammer, U., Peyrl, A., Jenne, D.E., Hansmann, I., Mautner, V.F. Am. J. Hum. Genet. (2004)
- Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17. Kehrer-Sawatzki, H., Schreiner, B., Tänzer, S., Platzer, M., Müller, S., Hameister, H. Am. J. Hum. Genet. (2002)
- Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1). Kehrer-Sawatzki, H., Wilda, M., Braun, V.M., Richter, H.P., Hameister, H. Acta Neuropathol. (2002)
- Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts. Kehrer-Sawatzki, H., Moschgath, E., Maier, C., Legius, E., Elgar, G., Krone, W. Gene (2000)
- Characterization of three genes, AKAP84, BAW and WSB1, located 3' to the neurofibromatosis type 1 locus in Fugu rubripes. Kehrer-Sawatzki, H., Maier, C., Moschgath, E., Elgar, G., Krone, W. Gene (1999)
- Genomic characterization of the Neurofibromatosis Type 1 gene of Fugu rubripes. Kehrer-Sawatzki, H., Maier, C., Moschgath, E., Elgar, G., Krone, W. Gene (1998)
- Mutational analysis and expression studies of the neurofibromatosis type 2 (NF2) gene in a patient with a ring chromosome 22 and NF2. Kehrer-Sawatzki, H., Udart, M., Krone, W., Baden, R., Fahsold, R., Thomas, G., Schmucker, B., Assum, G. Hum. Genet. (1997)
- A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2. Kehrer-Sawatzki, H., Schwickardt, T., Assum, G., Rocchi, M., Krone, W. Hum. Genet. (1997)