Impact of Fluorescent In Situ Hybridization Aberrations and CLLU1 Expression on the Prognosis of Chronic Lymphocytic Leukemia: Presentation of 156 Patients from Turkey by Abur, Ümmet, Oğur, Gönül, Akar, Ömer Salih, Altundağ, Engin, Aymelek, Huri Sema, Özatlı, Düzgün, Turgut, Mehmet

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Genetic burden and outcome of cystic hygromas detected antenatally: Results of 93 pregnancies from a single center in the Northern Region of Turkey by Aymelek, Huri, Oğur, Gönül, Tosun, Miǧraci, Abur, mmet, Altundaǧ, Engin, Çelik, Handan, Kurtoǧlu, Emel, Malatyalıoǧlu, Erdal, Akar, Ömer, Alper, Tayfun

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Genetic testing can change diagnosis and treatment in children with congenital hypothyroidism by Kara, Cengiz, Mammadova, Jamala, Abur, Ümmet, Gumuskaptan, Cagri, İzci Güllü, Elif, Dağdemir, Ayhan, Aydın, Murat

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Clinical, cytogenomic, and molecular characterization of isodicentric Y-chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe oligozoospermic i... by Abur, Ummet, Gunes, Sezgin, Hekim, Neslihan, Akar, Omer Salih, Altundag, Engin, Asci, Ramazan

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Correction to: Clinical, cytogenomic, and molecular characterization of isodicentric Y‑chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe ol... by Abur, Ummet, Gunes, Sezgin, Hekim, Neslihan, Akar, Omer Salih, Altundag, Engin, Asci, Ramazan

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Tr-KIT/c-KIT ratio in renal cell carcinoma by Ergün, Sercan, Altay, Diler Us, Güneş, Sezgin, Büyükalpelli, Recep, Karahan, Süleyman Caner, Tomak, Leman, Abur, Ümmet

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Which Ischemic Stroke Subtype Is Associated with Hyperhomocysteinemia? by Gungor, Levent, Polat, Murat, Ozberk, Mehlika Berra, Avci, Bahattin, Abur, Ummet

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Could familial Mediterranean fever gene mutations be related to PFAPA syndrome? by Celiksoy, Mehmet H., Ogur, Gonul, Yaman, Elif, Abur, Ummet, Fazla, Semanur, Sancak, Recep, Yildiran, Alisan

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Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation by Kutluğ, Seyhan, Ogur, Gönül, Yilmaz, Aysegül, Thijssen, Peter E., Abur, Ummet, Yildiran, Alisan

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Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence? by Ogur, Gonul, Kara, Cengiz, Yalcin, Hatice Yelda, Yilmaz, Aysegul, Altundag, Engin, Abur, Ummet, Baysal, Kemal, Aydin, Murat

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A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation by Abur, Ummet, Atmaca, Aysegul, Scott, Hamish, Gagliardi, Lucia, Altundag, Engin, Akar, Omer Salih, Bayrak, Ilkay Koray, Ogur, Gonul

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A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation by Abur, Ümmet, Atmaca, Ayşegül, Scott, Hamish, Gagliardi, Lucia, Altundağ, Engin, Akar, Ömer Salih, İlkay Koray Bayrak, Oğur, Gönül

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Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence? by Oğur, Gönül, Cengiz, Kara, Yalçın, Hatice Yelda, Yılmaz, Ayşegül, Altundağ, Engin, Abur, Ümmet, Baysal, Kemal, Aydın, Murat

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Evaluation of the promoter methylation status of hypoxia factor 3A and interleukin-6 genes and expression levels of mir-130b and mir-146b in childhood obesity by Tekcan, Esra, Kara, Nurten, Aydın, Hasan Murat, Abur, Ümmet, Abbaszadeh, Mohsen

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