Browsing by Author Semerci, C.Nur
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) |
|---|---|---|
| 2012 | Esansiyel hipertansiyonlu olgularda chromogranin A geni polimorfizmlerinin araştırılması | Eser, Metin |
| 2012 | Patient with 45,X karyotype and severe virilization occult y sequences | Çorduk, Nergül; Semiz, Serap ; Koltuksuz, Uğur ; Semerci, C.Nur; Düzcan, Füsun ; Düzcan, Ender; Şatıroğlu-Tufan, Naciye Lale |
| 2005 | Prenatal diagnosis of a trisomy 13 case associated with holoprosencephaly by ultrasonography and quantitative fluorescent PCR | Şatiroğlu Tufan; Tufan, Ahmet Çevik ; Yildirim, B.; Kaleli, Babür ; Semerci, C.Nur; Bir, Ferda ; Düzcan, Füsun ; Bağcı, Hüseyin |
| 2010 | Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome | Semerci, C.Nur; Cinbiş, Mine; Ullmann, R.; Steininger, A.; Bahce, M.; Yağcı, Baki ; Özden, Serap |