Approach in an adolescent Proteus male patient with megafoot by Orhan Derman, Sevim Balci, Ozlem Engiz

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An anencephalic monocephalus diprosopus "headed twin": postmortem and CT findings with emphasis on the cranial bones by Gazanfer Ekinci, Sevim Balci, Canan Erzen

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Variable expressivity of congenital longitudinal radial deficiency and spinal dysraphism in monozygotic twins by Gürsel Leblebicioğlu, Sevim Balci, Akin Uzümcügil

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Megalocornea, macrocephaly, mental and motor retardation: MMMM syndrome (Neuhäuser syndrome) in two sisters with hypoplastic corpus callosum by Sevim Balci, Ozlem Tekşam, Sansal Gedik

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A new case of omphalocele with absence of thumb by Sevim Balci, Gürsel Leblebicioğlu, Inci Yiğitkanli

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Succesful Management of the Pregnancy Complicated with Thrombophilia, Uterine Unicollis and Previous Pregnancy Loss: A Case Report by Sertaç Esin, Sinan Beksaç, Sevim Balcı

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Prenatally Diagnosed Ureteropelvic Junction Obstruction in Three Siblings of one Family: A Case Report by Sinan Beksaç, Sevim Balcı, Zuhal Yapıcı, Özgür Özyüncü

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A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome by Sevim Balci, Safak Güçer, Diclehan Orhan, Tevfik Karagöz

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The Mckusick-Kaufman syndrome: report of a case with some associations by Esin Kotiloğlu, Handan Kaya, Ilter Güney, Sevim Balci

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A 34-week-old male fetus with short rib polydactyly syndrome (SRPS) type I (Saldino-Noonan) with pancreatic cysts by Sevim Balci, Gülçin Altinok, Fulya Tekşen, Muzaffer Eryilmaz

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Effective treatment of multifocal aggressive fibromatosis with low-dose chemotherapy by Kudret Caglar, Hasan Ozyönüm, Minel Akalin, Sevim Balci

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Prenatally diagnosed case of 22q11.2 deletion syndrome associated with pulmonary artery aneurysm by Leyla Ozer, Arda Lembet, Nil Uğurlu, Volkan Baltaci, Sevim Balci

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Selective Feticide of The Aneuploid Fetus in a Twin Pregnancy: A Case Reports by Sinan Beksaç, Tülay Özlü, Sevim Balcı, Mehmet Alikaşifoğlu, Nur Çakar

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Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: a case report by Sevim Balci, Mehmet Ali Ergün, E Berrin Yüksel-Konuk, Oliver Bartsch

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A 13-year-old female with Turner syndrome and achalasia by Sevim Balci, Abdullah Bariş Akcan, Mehmet Emin Senocak, Arbay Ozden Ciftçi, Fatih Ozaltin

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Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies by Mehmet Ali Ergun, Sevim Balci, Ece Konaç, Derya Kan, Sevda Menevşe, Oliver Bartsch

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Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue by Diclehan Orhan, Sevim Balci, Ozgür Deren, Eda Gülen Utine, Ahmet Başaran, Gülsev Kale

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Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gest... by Sevim Balci, Fulya Tekşen, Fulya Dökmeci, Bora Cengiz, Ruhi Bariş Cömert, Bilge Can, Sükrü Ozdamar

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Genetic Counseling in a Case of a Pregnant Woman with Goldenhar Syndrome (Oculoauriculovertebral Spectrum) by Aslıhan Yazıcıoğlu, Özge Senem Yücel, İlker Selçuk, Gökhan Boyraz, Mert Turğal, Özgür Özyüncü, Sevim Balcı, Sinan Beksaç

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Cerebro-oculo-facio-skeletal syndrome: report of two cases from Turkey with postmortem findings by C Nur Semerci, Neşe Onat, Sevil Günçe, Nihal Demirel, Murat Becer Yanki Yilmazer, Izlem Oznur, Canan Türkyilmaz, Sevim Balci

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