| Title : Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization - Kopp_2020_Am.J.Med.Genet.A__e62025 |
| Author(s) : Kopp N , Amarillo I , Martinez-Agosto J , Quintero-Rivera F |
| Ref : American Journal of Medicine Genet A , :e62025 , 2020 |
| Abstract : Kopp_2020_Am.J.Med.Genet.A__e62025 |
| ESTHER : Kopp_2020_Am.J.Med.Genet.A__e62025 |
| PubMedSearch : Kopp_2020_Am.J.Med.Genet.A__e62025 |
| PubMedID: 33369065 |
| Gene_locus related to this paper: human-NLGN4X |
| Gene_locus related to this paper: human-NLGN4X |
Kopp N, Amarillo I, Martinez-Agosto J, Quintero-Rivera F (2020)
Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization
American Journal of Medicine Genet A
:e62025
Kopp N, Amarillo I, Martinez-Agosto J, Quintero-Rivera F (2020)
American Journal of Medicine Genet A
:e62025