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KARYOTYPIC DISTRIBUTION OF TURNER'S SYNDROME CASES

AYŞEGÜL ZAMANİ, SENNUR DEMIREL, HATİCE GÜL DURSUN, TÜLİN ÇORA, AYNUR ACAR

THE EVALUATION OF AMNIOCENTESIS CASES MADE FOR GENETIC EXAMINATION IN ONE-YEAR PERIOD

OSMAN BALCI, MURAT BÜYÜKDOĞAN, SUNA ÖZDEMİR, ALAA S. MAHMOUD, ALİ ACAR, AYŞEGÜL ZAMANİ

THE USE OF VASCULAR CLOSURE DEVICE IN PATIENTS WITH INTERVENTIONAL NEURORADIOLOGY: 4 YEARS EXPERIENCE

ORHAN ÖZBEK, OSMAN KOÇ, FATİH KESKİN, AHMET KÜÇÜKAPAN, İBRAHİM GÜLER, ALAATTİN VURAL

ANESTHESIA MANAGEMENT IN PETERS SYNDROME: A CASE REPORT

HAKAN ERKAL, METİN ÖZŞEKER, SÜLEYMAN DERMAN, BANU ELER ÇEVİK

LEFT VENTRICULAR DIVERTICULUM

AHMET SOYLU, MEHMET TOKAÇ, MEHMET AKİF DÜZENLİ

DEL11Q(13) IS A RARE CYTOGENETIC ABNORMALITY IN ACUTE MYELOID LEUKEMIA

EMİNE GÖKTAŞ, AYŞEGÜL ZAMANİ, AYNUR UĞUR BİLGİN, MAHMUT SELMAN YILDIRIM

A CASE WHO CARRIES RECIPROCAL TRANSLOCATION (18;20) (P11.3;Q11.2)

PELİN TAŞDEMİR, AYŞEGÜL ZAMANİ, SENNUR DEMIREL, AYNUR ACAR

GALLBLADDER AGENESIS, A RARE CONGENITAL DISORDER

MURAT ÇAKIR, TEVFİK KÜÇÜKKARTALLAR, AHMET TEKİN, ADİL KARTAL

THE ROLE OF CHROMOSOMAL ABNORMALITIES ON SPONTANEOUS ABORTIONS

HATİCE GÜL DURSUN, AYŞEGÜL ZAMANİ, AYNUR ACAR, MEHMET CENGİZ ÇOLAKOĞLU

INVESTIGATION OF PHENOTYPELKARYOTYPE COR-RELATION IN TWO CASES WITH TRISOMY 13

SENNUR DEMIREL, AYŞEGÜL ZAMANİ, TÜLİN ÇORA, HATİCE GÜL DURSUN, AYNUR ACAR

AN ABNORMALITY OF COMMON CAROTID ARTERY CAUSING DYSPHAGIA

ALI BAYRAM, YILMAZ KABAKKAYA, MUSTAFA BOLAT, ALAADDIN AVŞAR, ORHAN DEMİR

AN ABNORMALITY OF COMMON CAROTID ARTERY CAUSING DYSPHAGIA

ALI BAYRAM, YILMAZ KABAKKAYA, MUSTAFA BOLAT, ALAADDIN AVŞAR, ORHAN DEMİR

DUPLICATION OFTHE SMALL INTESTLNE.

YÜKSEL ARIKAN, FARUK AKSOY, İBRAHIM SUNGUR