| dc.contributor.author | Meester, JAN | en_US |
| dc.contributor.author | Southgate, L | en_US |
| dc.contributor.author | Stittrich, A-B | en_US |
| dc.contributor.author | Venselaar, H | en_US |
| dc.contributor.author | Beekmans, SJA | en_US |
| dc.contributor.author | den Hollander, N | en_US |
| dc.contributor.author | Bijlsma, EK | en_US |
| dc.contributor.author | den Enden, AH-V | en_US |
| dc.contributor.author | Verheij, JBGM | en_US |
| dc.contributor.author | Glusman, G | en_US |
| dc.contributor.author | Roach, JC | en_US |
| dc.contributor.author | Lehman, A | en_US |
| dc.contributor.author | Patel, MS | en_US |
| dc.contributor.author | de Vries, BBA | en_US |
| dc.contributor.author | Ruivenkamp, C | en_US |
| dc.contributor.author | Itin, P | en_US |
| dc.contributor.author | Prescott, K | en_US |
| dc.contributor.author | Clarke, S | en_US |
| dc.contributor.author | Trembath, R | en_US |
| dc.contributor.author | Zenker, M | en_US |
| dc.contributor.author | Sukalo, M | en_US |
| dc.contributor.author | Van Laer, L | en_US |
| dc.contributor.author | Loeys, B | en_US |
| dc.contributor.author | Wuyts, W | en_US |
| dc.date.accessioned | 2017-02-09T11:04:05Z | |
| dc.date.available | 2015-07-29 | en_US |
| dc.date.issued | 2015-09-03 | en_US |
| dc.date.submitted | 2017-02-08T12:04:02.042Z | |
| dc.identifier.issn | 0002-9297 | en_US |
| dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/19299 | |
| dc.description.sponsorship | B.L.L. is a senior clinical investigator of the Fund for Scientific
Research, Flanders and holds a European Reseach Council starting
grant. J.A.N.M. is a predoctoral researcher of the Fund for Scientific
Research, Flanders. A.B.S. was supported by the German Academic
480 The American Journal of Human Genetics 97, 475–482, September 3, 2015
Exchange Service and the German Research Foundation. This
research was supported by funding from the Fund for Scientific
Research, Flanders (G.0221.12), the Fondation Leducq, and the
European Research Council, a Center for Systems Biology P50
grant (GM076547, NIH), and the Rare Disease Foundation. | en_US |
| dc.format.extent | 475 - 482 | en_US |
| dc.relation.ispartof | AMERICAN JOURNAL OF HUMAN GENETICS | en_US |
| dc.rights | Under an Elsevier user license. | |
| dc.title | Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome | en_US |
| dc.type | Article | |
| dc.rights.holder | © 2015 The American Society of Human Genetics. Published by Elsevier Inc. | |
| dc.identifier.doi | 10.1016/j.ajhg.2015.07.015 | en_US |
| pubs.author-url | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000361084700010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
| pubs.issue | 3 | en_US |
| pubs.notes | Not known | en_US |
| pubs.publication-status | Published | en_US |
| pubs.volume | 97 | en_US |
