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American Journal of Medical Genetics|September 19, 1997
Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selectionR Schubert, R Viersbach, T Eggermann, et al.
Advances in Medical Sciences|July 11, 2008
Abnormalities in tooth morphology, structure and dentition in two children with chromosome aberrations. Translocation trisomy 13 and trisomy 21A Roos, T Eggermann, S Zschiesche, et al.
The Journal of Pediatrics|February 15, 2001
Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosomeG Binder, T Eggermann, H Enders, et al.
Human Genetics|April 1, 1997
Molecular investigation of the parental origin of a de novo unbalanced translocation 13/18T Eggermann, H Engels, C Heidrich-Kaul, et al.
Neuroscience|March 31, 2010
Medial temporal lobe dysfunction during encoding and retrieval of episodic memory in non-demented APOE epsilon4 carriersJ Kukolja, C M Thiel, T Eggermann, et al.
Orvosi Hetilap|August 10, 2001
[Uniparental disomy 7 in the pathogenesis of Silver-Russell syndrome]S Mergenthaler, M Dobos, H Wollmann, et al.
Hormone Research in Paediatrics|September 21, 2013
Adult height and epigenotype in children with Silver-Russell syndrome treated with GHG Binder, M Liebl, J Woelfle, et al.
European Journal of Neurology|April 18, 2007
Mitofusin 2 gene mutation (R94Q) causing severe early-onset axonal polyneuropathy (CMT2A)C Neusch, J Senderek, T Eggermann, et al.
Molecular Syndromology|July 26, 2013
Haploinsufficiency of ANKRD11 (16q24.3) Is Not Obligatorily Associated with Cognitive Impairment but Shows a Clinical Overlap with Silver-Russell SyndromeS Spengler, B Oehl-Jaschkowitz, M Begemann, et al.
Cytogenetic and Genome Research|July 11, 2006
Two complementary recombinant chromosomes 5 in a healthy womanO Bartsch, M A Ergun, S Balci, et al.
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