| dc.contributor.author | Gallagher, Louise | en |
| dc.contributor.author | Lynch, Sally | en |
| dc.date.accessioned | 2018-08-23T11:14:01Z | |
| dc.date.available | 2018-08-23T11:14:01Z | |
| dc.date.issued | 2019 | en |
| dc.date.submitted | 2019 | en |
| dc.identifier.citation | Al Shehhi, M. and Forman, E.B. and Fitzgerald, J.E. and McInerney, V. and Krawczyk, J. and Shen, S. and Betts, D.R. and Ardle, L.M. and Gorman, K.M. and King, M.D. and Green, A. and Gallagher, L. and Lynch, S.A., NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families, European Journal of Medical Genetics, 62, 3, 2019, 204-209 | en |
| dc.identifier.other | Y | en |
| dc.description | PUBLISHED | en |
| dc.description | cited By 0; Article in Press | en |
| dc.format.extent | 204-209 | en |
| dc.relation.ispartofseries | European Journal of Medical Genetics | en |
| dc.relation.ispartofseries | 62 | en |
| dc.relation.ispartofseries | 3 | en |
| dc.rights | Y | en |
| dc.title | NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families | en |
| dc.type | Journal Article | en |
| dc.type.supercollection | scholarly_publications | en |
| dc.type.supercollection | refereed_publications | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/lgallagh | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/lynchs17 | en |
| dc.identifier.rssinternalid | 191422 | en |
| dc.identifier.doi | http://dx.doi.org/10.1016/j.ejmg.2018.07.015 | en |
| dc.rights.ecaccessrights | openAccess | |
| dc.identifier.orcid_id | 0000-0001-9462-2836 | en |
| dc.identifier.uri | http://hdl.handle.net/2262/83971 | |
