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Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients

dc.contributor.authorUludag, D.
dc.contributor.authorErcan-Sencicek, G.
dc.contributor.authorBilguvar, K.
dc.contributor.authorAkdeniz, B.
dc.contributor.authorTuysuz, B.
dc.contributor.authorGunes, N.
dc.contributor.authorCaglayan, O.
dc.date.accessioned2021-03-02T22:01:03Z
dc.date.available2021-03-02T22:01:03Z
dc.identifier.citationAkdeniz 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.othervv_1032021
dc.identifier.otherav_0a33059a-f834-48f3-ab88-c6cf2559057b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/12613
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectTemel Bilimler
dc.subjectSitogenetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.titleSevere speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients
dc.typeBildiri
dc.contributor.departmentYale University , ,
dc.identifier.volume27
dc.contributor.firstauthorID156404


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