| Title : Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters - Harrison_2011_Am.J.Med.Genet.A_155A_2826 |
| Author(s) : Harrison V , Connell L , Hayesmoore J , McParland J , Pike MG , Blair E |
| Ref : American Journal of Medicine Genet A , 155A :2826 , 2011 |
| Abstract : Harrison_2011_Am.J.Med.Genet.A_155A_2826 |
| ESTHER : Harrison_2011_Am.J.Med.Genet.A_155A_2826 |
| PubMedSearch : Harrison_2011_Am.J.Med.Genet.A_155A_2826 |
| PubMedID: 21964664 |
Harrison V, Connell L, Hayesmoore J, McParland J, Pike MG, Blair E (2011)
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
American Journal of Medicine Genet A
155A :2826
Harrison V, Connell L, Hayesmoore J, McParland J, Pike MG, Blair E (2011)
American Journal of Medicine Genet A
155A :2826