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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 6
2016
Mehraein, Yasmin; Schmid, Irene; Eggert, Marlene; Kohlhase, Jürgen und Steinlein, Ortrud K.
(2016):
DICER1 syndrome can mimic different genetic tumor predispositions.
In: Cancer Letters, Bd. 370, Nr. 2: S. 275-278
Korenke, Georg-Christoph; Eggert, Marlene; Thiele, Holger; Nürnberg, Peter; Sander, Thomas und Steinlein, Ortrud K.
(2016):
Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3.
In: Epilepsia, Bd. 57, Nr. 3, E60-E63
Eggert, Marlene; Müller, Stefan; Heinrich, Uwe und Mehraein, Yasmin
(2016):
A new familial case of microdeletion syndrome 10p15.3.
In: European Journal of Medical Genetics, Bd. 59, Nr. 4: S. 179-182
2015
Eggert, Marlene; Winterer, Georg; Wanischeck, Mario; Hoda, Jean-Charles; Bertrand, Daniel und Steinlein, Ortrud K.
(2015):
The nicotinic acetylcholine receptor alpha 4 subunit contains a functionally relevant SNP Haplotype.
In: BMC Genetics
16:46
[PDF, 540kB]
Mehraein, Yasmin; Pfob, Martina; Steinlein, Ortrud K.; Aichinger, Eric; Eggert, Marlene; Bubendorff, Valerie; Mannhart, Adelina und 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, Bd. 146, Nr. 1: S. 33-38
[PDF, 405kB]
2013
Eggert, Marlene; Pfob, Martina und Steinlein, Ortrud K.
(2013):
Melanocortin-3-receptor promoter polymorphism associated with tuberculosis susceptibility does not influence protein expression.
In: BMC Research Notes
6:99
[PDF, 146kB]