dc.contributor.author | Uludag, D. | |
dc.contributor.author | Ercan-Sencicek, G. | |
dc.contributor.author | Bilguvar, K. | |
dc.contributor.author | Akdeniz, B. | |
dc.contributor.author | Tuysuz, B. | |
dc.contributor.author | Gunes, N. | |
dc.contributor.author | Caglayan, O. | |
dc.date.accessioned | 2021-03-02T22:01:03Z | |
dc.date.available | 2021-03-02T22:01:03Z | |
dc.identifier.citation | Akdeniz B., Gunes N., Uludag D., Ercan-Sencicek G., Caglayan O., Bilguvar K., Tuysuz B., "Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients", 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.315-316 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_0a33059a-f834-48f3-ab88-c6cf2559057b | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/12613 | |
dc.language.iso | eng | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıbbi Genetik | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | BİYOKİMYA VE MOLEKÜLER BİYOLOJİ | |
dc.subject | Temel Bilimler | |
dc.subject | Sitogenetik | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | GENETİK VE HAYAT | |
dc.title | Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients | |
dc.type | Bildiri | |
dc.contributor.department | Yale University , , | |
dc.identifier.volume | 27 | |
dc.contributor.firstauthorID | 156404 | |