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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 6

Zeitschriftenartikel

Mehraein, Yasmin; Schmid, Irene; Eggert, Marlene; Kohlhase, Jürgen; Steinlein, Ortrud K. (2016): DICER1 syndrome can mimic different genetic tumor predispositions. In: Cancer Letters, Vol. 370, Nr. 2: S. 275-278

Korenke, Georg-Christoph; Eggert, Marlene; Thiele, Holger; Nürnberg, Peter; Sander, Thomas; Steinlein, Ortrud K. (2016): Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3. In: Epilepsia, Vol. 57, Nr. 3, E60-E63

Eggert, Marlene; Müller, Stefan; Heinrich, Uwe; Mehraein, Yasmin (2016): A new familial case of microdeletion syndrome 10p15.3. In: European Journal of Medical Genetics, Vol. 59, Nr. 4: S. 179-182

Eggert, Marlene; Winterer, Georg; Wanischeck, Mario; Hoda, Jean-Charles; Bertrand, Daniel; Steinlein, Ortrud K.: The nicotinic acetylcholine receptor alpha 4 subunit contains a functionally relevant SNP Haplotype. In: BMC Genetics 2015, 16:46 [PDF, 540kB]

Mehraein, Yasmin; Pfob, Martina; Steinlein, Ortrud K.; Aichinger, Eric; Eggert, Marlene; Bubendorff, Valerie; Mannhart, Adelina; Müller, Stefan (2015): 2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3. In: Cytogenetic and Genome Research, Vol. 146, Nr. 1: S. 33-38 [PDF, 405kB]

Eggert, Marlene; Pfob, Martina; Steinlein, Ortrud K.: Melanocortin-3-receptor promoter polymorphism associated with tuberculosis susceptibility does not influence protein expression. In: BMC Research Notes 2013, 6:99 [PDF, 146kB]

Diese Liste wurde am Wed Mar 20 03:00:22 2019 CET erstellt.