|
|||||
|
|
Microdeletion 1p35.2: A recognizable facial phenotype with developmental delay |
|
| Authors: | Brian T. Wilson Murwan Omer Stephen W. Hellens Simon A. Zwolinski Laura M. Yates Sally Ann Lynch |
| Affiliation: | 1. Institute of Genetic Medicine, Newcastle University, International Centre for Life, Newcastle upon Tyne, UK;2. Northern Genetics Service, Newcastle upon Tyne Hospitals NHS Foundation Trust, International Centre for Life, Newcastle upon Tyne, UK;3. National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Ireland |
| Abstract: | |
| Keywords: | deletion 1p35.2 HDAC1 histone deacetylase karyopherin alpha 6 (importin alpha 7) human |