Hasil Pencarian - Seher Başaran
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Non-Mosaic Tetrasomy 9p in An Infant With Multiple Congenital Anomalies oleh Füsun Düzcan, Hacer Ergin, Melike Aytan, Emre Tepeli, Özmert Özdemir, Seher Başaran
Diterbitkan 2007-08-01Dapatkan teks lengkap
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Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD oleh Neşe Akcan, Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy, Birsen Karaman, Şahin Avcı, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendeliler
Diterbitkan 2022-06-01Dapatkan teks lengkap
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4
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency oleh Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, Birsen Karaman, Güven Toksoy, Şükran Poyrazoğlu, Şahin Avcı, Umut Altunoğlu, Zehra Yavaş Abalı, Ayşe Pınar Öztürk, Esin Karakılıç Özturan, Seher Başaran, Feyza Darendeliler, Z. Oya Uyguner
Diterbitkan 2023-12-01Dapatkan teks lengkap
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5
Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases oleh Asuman Gedikbasi, Asuman Gedikbasi, Guven Toksoy, Meryem Karaca, Cagri Gulec, Mehmet Cihan Balci, Dilek Gunes, Seda Gunes, Ayca Dilruba Aslanger, Gokcen Unverengil, Birsen Karaman, Birsen Karaman, Seher Basaran, Mubeccel Demirkol, Gulden Fatma Gokcay, Zehra Oya Uyguner
Diterbitkan 2023-06-01Dapatkan teks lengkap
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