Browsing by Author Ayter, Şükriye
Showing results 1 to 9 of 9
| Issue Date | Title | Author(s) |
|---|---|---|
| Feb-2018 | Clinical findings and mutation analysis of NF1 patients in Turkey | Terzi, Yunus Kasım; Balcı, Sibel Oğuzkan; Anlar, Banu; Varan, Ali; Evans, Sibel Ersoy; Sharafi, Parisa ; Ayter, Şükriye |
| 2023 | Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in Turkey | Sharafi, Parisa ; Varan, Ali; Ersoy-Evans, Sibel; Ayter, Şükriye |
| 1-Jul-2018 | The effect of parental age on NF1 patients in Turkey | Ersoy, Evans Sibel; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Yılmaz, Ömer Faruk; Turan, Mustafa ; Ayter, Şükriye |
| 1-May-2018 | Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas | Karaosmanoğlu, Beren; Kocaefe, Çetin Y.; Söylemezoğlu, Figen; Anlar, Banu; Varan, Ali; Vargel, İbrahim; Ayter, Şükriye |
| 2019 | Lösemiler ve NF1 ile İlişkili Tümörlerde EVI2A ve EVI2B Genlerinin Rolü | Ayter, Şükriye ; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Çetin, Mualla |
| May-2017 | NF1 Gene Mutations are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome | Sharafi, Parisa ; Anlar, Banu; Ayter, Şükriye |
| Oct-2013 | Phacomatosis | Ayter, Şükriye |
| 3-Apr-2018 | Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes | Sharafi, Parisa ; Ayter, Şükriye |
| 2020 | Yapay Zekâ ve Genetik | Ayter, Şükriye ; Sharafi, Parisa |