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Title : Serum paraoxonase level and paraoxonase polymorphism in patients with acromegaly - Arpaci_2016_Redox.Rep__1 |
Author(s) : Arpaci D , Karakas Celik S , Can M , Ermis E , Kuzu F , Kokturk F , Hamamcioglu AC , Dursun A , Bayraktaroglu T |
Ref : Redox Rep , :1 , 2016 |
Abstract : Arpaci_2016_Redox.Rep__1 |
ESTHER : Arpaci_2016_Redox.Rep__1 |
PubMedSearch : Arpaci_2016_Redox.Rep__1 |
PubMedID: 26863932 |
Title : Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388 |
Author(s) : Unal O , Ozgul RK , Yucel D , Yalnizoglu D , Tokatli A , Sivri HS , Hismi B , Coskun T , Dursun A |
Ref : Turk J Pediatr , 57 :388 , 2015 |
Abstract : Unal_2015_Turk.J.Pediatr_57_388 |
ESTHER : Unal_2015_Turk.J.Pediatr_57_388 |
PubMedSearch : Unal_2015_Turk.J.Pediatr_57_388 |
PubMedID: 27186703 |
Gene_locus related to this paper: human-SERAC1 |