Report for Yuksel A

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References (2)

Title : A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing - Alagoz_2020_Exp.Ther.Med_19_3505
Author(s) : Alagoz M , Kherad N , Turkmen S , Bulut H , Yuksel A
Ref : Exp Ther Med , 19 :3505 , 2020
Abstract : Alagoz_2020_Exp.Ther.Med_19_3505
ESTHER : Alagoz_2020_Exp.Ther.Med_19_3505
PubMedSearch : Alagoz_2020_Exp.Ther.Med_19_3505
PubMedID: 32346411
Gene_locus related to this paper: human-SERAC1

Title : Prenatal diagnosis of diastematomyelia: presentation of eight cases and review of the literature - Has_2007_Ultrasound.Obstet.Gynecol_30_845
Author(s) : Has R , Yuksel A , Buyukkurt S , Kalelioglu I , Tatli B
Ref : Ultrasound Obstet Gynecol , 30 :845 , 2007
Abstract : Has_2007_Ultrasound.Obstet.Gynecol_30_845
ESTHER : Has_2007_Ultrasound.Obstet.Gynecol_30_845
PubMedSearch : Has_2007_Ultrasound.Obstet.Gynecol_30_845
PubMedID: 17726726