Results
|
1061.
|
|
|
1062.
|
|
|
1063.
|
Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome. [electronic resource] by
- Kolanczyk, Mateusz
- Krawitz, Peter
- Hecht, Jochen
- Hupalowska, Anna
- Miaczynska, Marta
- Marschner, Katrin
- Schlack, Claire
- Emmerich, Denise
- Kobus, Karolina
- Kornak, Uwe
- Robinson, Peter N
- Plecko, Barbara
- Grangl, Gernot
- Uhrig, Sabine
- Mundlos, Stefan
- Horn, Denise
Producer: 20160106
In:
European journal of human genetics : EJHG vol. 23
Availability: No items available.
|
|
1064.
|
|
|
1065.
|
|
|
1066.
|
|
|
1067.
|
|
|
1068.
|
|
|
1069.
|
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression. [electronic resource] by
- Frank, Valeska
- Habbig, Sandra
- Bartram, Malte P
- Eisenberger, Tobias
- Veenstra-Knol, Hermine E
- Decker, Christian
- Boorsma, Reinder A C
- Göbel, Heike
- Nürnberg, Gudrun
- Griessmann, Anabel
- Franke, Mareike
- Borgal, Lori
- Kohli, Priyanka
- Völker, Linus A
- Dötsch, Jörg
- Nürnberg, Peter
- Benzing, Thomas
- Bolz, Hanno J
- Johnson, Colin
- Gerkes, Erica H
- Schermer, Bernhard
- Bergmann, Carsten
Producer: 20131230
In:
Human molecular genetics vol. 22
Availability: No items available.
|