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The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism? [electronic resource] by
- Eggermann, Thomas
- Oehl-Jaschkowitz, Barbara
- Dicks, Severin
- Thomas, Wolfgang
- Kanber, Deniz
- Albrecht, Beate
- Begemann, Matthias
- Kurth, Ingo
- Beygo, Jasmin
- Buiting, Karin
Producer: 20180119
In:
Molecular genetics & genomic medicine vol. 5
Availability: No items available.
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36.
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Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contractures. [electronic resource] by
- Elbracht, Miriam
- Kraft, Florian
- Begemann, Matthias
- Holschbach, Petra
- Mull, Michael
- Kabat, Ildiko M
- Müller, Britta
- Häusler, Martin
- Kurth, Ingo
- Hehr, Ute
Producer: 20190123
In:
Molecular genetics & genomic medicine vol. 6
Availability: No items available.
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37.
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Paternally Inherited IGF2 Mutation and Growth Restriction. [electronic resource] by
- Begemann, Matthias
- Zirn, Birgit
- Santen, Gijs
- Wirthgen, Elisa
- Soellner, Lukas
- Büttel, Hans-Martin
- Schweizer, Roland
- van Workum, Wilbert
- Binder, Gerhard
- Eggermann, Thomas
Producer: 20150804
In:
The New England journal of medicine vol. 373
Availability: No items available.
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38.
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Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32. [electronic resource] by
- Beygo, Jasmin
- Elbracht, Miriam
- de Groot, Karel
- Begemann, Matthias
- Kanber, Deniz
- Platzer, Konrad
- Gillessen-Kaesbach, Gabriele
- Vierzig, Anne
- Green, Andrew
- Heller, Raoul
- Buiting, Karin
- Eggermann, Thomas
Producer: 20150929
In:
European journal of human genetics : EJHG vol. 23
Availability: No items available.
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39.
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Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation. [electronic resource] by
- Bohne, Florian
- Langer, David
- Martiné, Ursula
- Eider, Claudia S
- Cencic, Regina
- Begemann, Matthias
- Elbracht, Miriam
- Bülow, Luzie
- Eggermann, Thomas
- Zechner, Ulrich
- Pelletier, Jerry
- Zabel, Bernhard Ulrich
- Enklaar, Thorsten
- Prawitt, Dirk
Producer: 20161214
In:
Clinical epigenetics vol. 8
Availability: No items available.
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40.
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Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features. [electronic resource] by
- Spengler, Sabrina
- Begemann, Matthias
- Ortiz Brüchle, Nadina
- Baudis, Michael
- Denecke, Bernd
- Kroisel, Peter Michael
- Oehl-Jaschkowitz, Barbara
- Schulze, Bernd
- Raabe-Meyer, Gisela
- Spaich, Christiane
- Blümel, Peter
- Jauch, Anna
- Moog, Ute
- Zerres, Klaus
- Eggermann, Thomas
Producer: 20130110
In:
The Journal of pediatrics vol. 161
Availability: No items available.
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