Markus Hengstschläger
Department of Prenatal Diagnosis and Therapy
University of Vienna
Austria
Name/email consistency: high
- Patient with partial trisomy 9q and learning disability but no pyloric stenosis. Hengstschläger, M., Prusa, A.R., Repa, C., Drahonsky, R., Deutinger, J., Pollak, A., Bernaschek, G. Dev. Med. Child. Neurol (2004)
- Prenatal diagnosis of tetrasomy 9p with Dandy-Walker malformation. Hengstschläger, M., Bettelheim, D., Drahonsky, R., Repa, C., Deutinger, J., Bernaschek, G. Prenat. Diagn. (2004)
- Sex chromosome aberrations and transsexualism. Hengstschläger, M., van Trotsenburg, M., Repa, C., Marton, E., Huber, J.C., Bernaschek, G. Fertil. Steril. (2003)
- Prenatal diagnosis of a de novo inversion of chromosome (2)(p21q11). Hengstschläger, M., Mittermayer, C., Prusa, A.R., Drahonsky, R., Repa, C., Deutinger, J., Bernaschek, G. Arch. Gynecol. Obstet. (2003)
- Prenatal diagnosis of a supernumerary aberrant chromosome 9. Hengstschläger, M., Bettelheim, D., Dörfler-Grassauer, D., Prusa, A.R., Drahonsky, R., Deutinger, J., Bernaschek, G. Arch. Gynecol. Obstet. (2003)
- Tuberous sclerosis gene products in proliferation control. Hengstschläger, M., Rodman, D.M., Miloloza, A., Hengstschläger-Ottnad, E., Rosner, M., Kubista, M. Mutat. Res. (2001)
- Tuberous sclerosis complex genes: from flies to human genetics. Hengstschläger, M. Arch. Dermatol. Res. (2001)
- Cyclin-dependent kinases at the G1-S transition of the mammalian cell cycle. Hengstschläger, M., Braun, K., Soucek, T., Miloloza, A., Hengstschläger-Ottnad, E. Mutat. Res. (1999)
- Fetal cells in the peripheral blood of pregnant women express thymidine kinase: a new marker for detection. Hengstschläger, M., Bernaschek, G. FEBS Lett. (1997)