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Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.American Journal of Medical Genetics|March 7, 1998
New case of mosaic tetrasomy 9p with additional neurometabolic findingsT Eggermann, E Rossier, U Theurer-Mainka, et al.Clinical Genetics|December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndromeT Eggermann, N Schönherr, K Eggermann, et al.Human Genetics|September 1, 1997
Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomyT Eggermann, H A Wollmann, R Kuner, et al.The Journal of Clinical Endocrinology and Metabolism|August 31, 2006
IGF-II serum levels are normal in children with Silver-Russell syndrome who frequently carry epimutations at the IGF2 locusG Binder, A-K Seidel, K Weber, et al.Orvosi Hetilap|August 30, 2000
[Aberrations of chromosome 18 and their significance in genetic counseling]T Eggermann, G Bujdosó, T Haug, et al.Clinical Genetics|December 30, 2016
Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itselfR Scheuvens, M Begemann, L Soellner, et al.Journal of Medical Genetics|May 3, 2005
Is maternal duplication of 11p15 associated with Silver-Russell syndrome?T Eggermann, E Meyer, C Obermann, et al.Fortschritte Der Medizin. Originalien|April 9, 2002
[Molecular biology of cystinuria]A Albers, C A Wagner, C Schmidt, et al.Clinical Genetics|July 3, 1998
Molecular and cytogenetic [correction of cytogenate] analysis of an X/autosomal translocation: 45,X,dic(X;17)(p22.2;p13)T Eggermann, U Mau, U Klein-Vogler, et al.Pageof 7