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 : |
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 : |
PubMedSearch : Has_2007_Ultrasound.Obstet.Gynecol_30_845 |
PubMedID: 17726726 |