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| Title : Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families - Egger_2014_Neurogenetics_15_117 |
| Author(s) : Egger G , Roetzer KM , Noor A , Lionel AC , Mahmood H , Schwarzbraun T , Boright O , Mikhailov A , Marshall CR , Windpassinger C , Petek E , Scherer SW , Kaschnitz W , Vincent JB |
| Ref : Neurogenetics , 15 :117 , 2014 |
| Abstract : Egger_2014_Neurogenetics_15_117 |
| ESTHER : Egger_2014_Neurogenetics_15_117 |
| PubMedSearch : Egger_2014_Neurogenetics_15_117 |
| PubMedID: 24643514 |
| Title : Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures - Lionel_2013_Hum.Mol.Genet_22_2055 |
| Author(s) : Lionel AC , Vaags AK , Sato D , Gazzellone MJ , Mitchell EB , Chen HY , Costain G , Walker S , Egger G , Thiruvahindrapuram B , Merico D , Prasad A , Anagnostou E , Fombonne E , Zwaigenbaum L , Roberts W , Szatmari P , Fernandez BA , Georgieva L , Brzustowicz LM , Roetzer K , Kaschnitz W , Vincent JB , Windpassinger C , Marshall CR , Trifiletti RR , Kirmani S , Kirov G , Petek E , Hodge JC , Bassett AS , Scherer SW |
| Ref : Hum Mol Genet , 22 :2055 , 2013 |
| Abstract : Lionel_2013_Hum.Mol.Genet_22_2055 |
| ESTHER : Lionel_2013_Hum.Mol.Genet_22_2055 |
| PubMedSearch : Lionel_2013_Hum.Mol.Genet_22_2055 |
| PubMedID: 23393157 |