Expression of the syncytin-1 and syncytin-2 genes in the trophoblastic tissue of the early pregnancy losses with normal and abnormal karyotypes von Tug, Esra, Yirmibes Karaoguz, Meral, Nas, Tuncay

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Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies? von YURTCU, Erkan, KARÇAALTINCABA, Deniz, KAZAN, Hasan Hüseyin, ÖZDEMİR, Halis, YİRMİBEŞ KARAOĞUZ, Meral, ÇALIŞ, Pınar, KAYHAN, Gülsüm, GÜNTEKİN ERGÜN, Sezen, PERÇİN, Ferda, BAYRAM, Merih, İLHAN, Mustafa Necmi, BİLGİLİ, Gamze, KAYMAK, Tuğrul, ERGÜN, Mehmet Ali

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Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings von Kayhan, Gülsüm, Cavdarli, Büsranur, Yirmibes Karaoguz, Meral, Percin, E. Ferda, Oztürk Kaymak, Aysegül, Biri, Aydan, Ergun, M. Ali

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A Rare Prenatal Case: Greig Cephalopolysyndactyly Syndrome von Hakçıl, Tilbe, Kayhan, Gülsüm, Nas, Tuncay, Telli Celtemen, Pınar, Yirmibeş Karaoğuz, Meral

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Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnormal first trimester screening and choroid plexus cyst detected on ultrasound von Koç, Altuğ, Arısoy, Özgür, Pala, Elif, Erdem, Mehmet, Kaymak, Ayşegül Öztürk, Erkal, Özgür, Karaoğuz, Meral Yirmibeş

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The interrelation between the high expression level of MIR34a and the trisomic abortion materials von Kazancioglu, Elvin, Tug, Esra, Ergun, Mehmet Ali, Kazan, Hasan Huseyin, Karaoguz, Meral Yirmibes

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A prenatal tertiary trisomy resulting from balanced maternal 8; 9 translocation von Kayhan, Gulsum, Ergun, Mehmet Ali, Asyali Biri, Aydan, Yirmibes Karaoguz, Meral

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Monosomy 1p36 Syndrome: The First Case Report from Turkey von KARAER, Kadri, KARAOĞUZ, Meral Y., PERÇİN, E. Ferda

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AN UNBALANCED PRODUCT DUE TO A MATERNAL RECIPROKAL ADJACENT-2 SEGREGATION CASE WITH DICENTRIC PARTIAL TRISOMY 9/ MATERNAL RESIPROKAL TRANSLOKASYONUN ADJACENT-2 SEGREGASYONUNA BAGLI... von Urtekin, Ezgi, Kayhan, Gulsum, Kazancioglu, Elvin, Karaoguz, Meral Yirmibes

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Gastroschisis with Fetal Chromosomal Abnormality: A Case Report von Guler, Ismail, Erdem, Ahmet, Biri, Aydan, Gunaydin, Guven, Yilmaz, Ercan, Erdem, Mehmet, Karaoguz, Meral Yirmibeş

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Is cytogenetic diagnosis of 46,XX karyotype spontaneous abortion specimens erroneous? Fluorescence in situ hybridization as a confirmatory technique von Karaoguz, Meral Yirmibes, Nas, Tuncay, Konaç, Ece, Ince, Didem, Pala, Elif, Menevse, Sevda

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Diagnostic Yield of Molecular Karyotyping of Idiopathic Intellectual Disability Patients Ended with One Causative Anomaly; Duplication 9q34 Syndrome von Çavdarlı,Büşranur, Perçin,Emriye Ferda, Yirmibeş Karaoğuz,Meral, Ergün,Mehmet Ali

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Holoprosencephaly: A Rare Finding in Mosaic Trisomy 9 Syndrome von Mermer, Serdar, Ozek, Murat, Percin, Ferda, Karaoguz, Meral, Bayram, Merih

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Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing von Bakır, Abdullatif, Yirmibeş Karaoğuz, Meral, Perçin, Ferda Emriye, Tuğ, Esra, Cinaz, Peyami, Ergün, Mehmet Ali

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Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case von Tuğ, Esra, Yirmibeş Karaoğuz, Meral, Kayhan, Gülsüm, Ergün, Mehmet Ali, Perçin, Ferda E.

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Diagnosis of the Genomic Imprinting Diseases by the Usage of Conventional and Molecular Analyses von Öztürk Kaymak,Ayşegül, Gücüyener,Kıvılcım, Yirmibeş Karaoğuz,Meral, Perçin,Emriye Ferda

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Thrombophilic Status of Extracted Fetal Tissues of Spontaneously Aborted Embroys von Erdem,Ahmet, Balabanlı,Kanuni Barbaros, Pala,Elif, Yirmibeş Karaoğuz,Meral, Perçin,Emriye Ferda

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An unexpected finding in a child with neurological problems: mosaic ring chromosome 18 von Koç, Altuğ, Kan, Derya, Karaer, Kadri, Ergün, Mehmet A., Karaoğuz, Meral Yirmibeş, Gücüyener, Kıvılcım, Hinreiner, Sophie, Liehr, Thomas, Perçin, E. Ferda

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Apolipoprotein E Gene Polymorphism in Nonalcoholic Fatty Liver Disease von DEMIRAG, Mehmet Derya, ONEN, Hacer Iike, KARAOGUZ, Meral Yirmibes, DOGAN, Ibrahim, KARAKAN, Tarkan, EKMEKCI, Abdullah, GUZ, Galip

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Detection of Marker Chromosome in the Abortion Material; Does It Reflect the Karyotype of the Pregnancy Lost Tissue or the Maternal Decidual Tissue? Case Report von KOÇ, Altuğ, YİRMİBEŞ KARAOĞUZ, Meral, PALA, Elif, PERÇİN, E. Ferda, ERDEM, Mehmet, KARAER, Kadri, ÖZTÜRK KAYMAK, Ayşegül

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