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Author/Creator Topa, Alexandra

2. CTNND2—a candidate gene for reading problems and mild intellectual disability. Issue 2 (3rd December 2014)

Authors:
Hofmeister, Wolfgang; Nilsson, Daniel; Topa, Alexandra; Anderlid, Britt-Marie; Darki, Fahimeh; Matsson, Hans; Tapia Páez, Isabel; Klingberg, Torkel; Samuelsson, Lena; Wirta, Valtteri; Vezzi, Francesco; Kere, Juha; Nordenskjöld, Magnus; Syk Lundberg, Elisabeth; Lindstrand, Anna
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 2(2015)
Page Start:
111
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Different mutations in PDE4D associated with developmental disorders with mirror phenotypes. Issue 1 (7th November 2013)

Authors:
Lindstrand, Anna; Grigelioniene, Giedre; Nilsson, Daniel; Pettersson, Maria; Hofmeister, Wolfgang; Anderlid, Britt-Marie; Kant, Sarina G.; Ruivenkamp, Claudia A L; Gustavsson, Peter; Valta, Helena; Geiberger, Stefan; Topa, Alexandra; Lagerstedt-Robinson, Kristina; Taylan, Fulya; Wincent, Josephin...
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 1(2014)
Page Start:
45
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗