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Author/Creator Göhring, Ina

1. Cohen syndrome diagnosis using whole genome arrays. Issue 2 (4th October 2010)

Authors:
Rivera-Brugués, Nuria; Albrecht, Beate; Wieczorek, Dagmar; Schmidt, Heinrich; Keller, Thomas; Göhring, Ina; Ekici, Arif B; Tzschach, Andreas; Garshasbi, Masoud; Franke, Kathlen; Klopp, Norman; Wichmann, H-Erich; Meitinger, Thomas; Strom, Tim M; Hempel, Maja
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 2(2011)
Page Start:
136
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Disruption of ST5 is associated with mental retardation and multiple congenital anomalies. Issue 2 (19th October 2009)

Authors:
Göhring, Ina; Tagariello, Andreas; Endele, Sabine; Stolt, Claus C; Ghassibé, Michella; Fisher, Malcolm; Thiel, Christian T; Trautmann, Udo; Vikkula, Miikka; Winterpacht, Andreas; FitzPatrick, David R; Rauch, Anita
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 2(2010)
Page Start:
91
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays. Issue 10 (29th June 2007)

Authors:
Hoyer, Juliane; Dreweke, Alexander; Becker, Christian; Göhring, Ina; Thiel, Christian T; Peippo, Maarit M; Rauch, Ralf; Hofbeck, Michael; Trautmann, Udo; Zweier, Christiane; Zenker, Martin; Hüffmeier, Ulrike; Kraus, Cornelia; Ekici, Arif B; Rüschendorf, Franz; Nürnberg, Peter; Reis, André; Rauch,...
Journal:
Journal of medical genetics
Issue:
Volume 44:Issue 10(2007)
Page Start:
629
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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