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المؤلفون: Zehra Kara, Özge Şahin Kimyon, Batuhan Bulan, Kübra Akkaya, Cem Sulu, Ahmet Numan Demir, Serhat Uysal, Serdar Arslan, Hande Mefkure Özkaya, Pınar Kadıoğlu
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::684b195bd754cde022552eca4c8c8a40
https://doi.org/10.21203/rs.3.rs-2540359/v1 -
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المؤلفون: Aydan Akdeniz, Ayşegül Ünüvar, Muhlis Cem Ar, Esra Pekpak, Arzu Akyay, Özgür Mehtap, Fatma Keklik Karadağ, Can Acıpayam, Ali Doğan, Ömer Ekinci, Sultan Aydın Köker, Canan Albayrak, Ufuk Demirci, Tekin Güney, Meltem Kurt, Serap Karaman, Özge Şahin Kimyon, Sinan Albayrak, Yurday Öncül, Serkan Ünal, Fahri Şahin, Rumeysa Tuna, Bulent Zulfikar, Burcu Belen Apak, Elif Gülsüm Ümit, Ahmet Muzaffer Demir
المصدر: Scandinavian Journal of Clinical and Laboratory Investigation. 82:28-36
مصطلحات موضوعية: Turkey, Genotype, Prophylaxis, Factor VII Deficiency, Clinical Biochemistry, rare diseases, General Medicine, Factor VII, blood coagulation disorder, Severity, Phenotypes, Blood Coagulation Disorders, Inherited, Diagnosis, Symptoms, Humans, FVII deficiency, Women, Registries, hemorrhage, Rare Coagulation Disorders, Bleeding Disorders