Prenatal Diagnosis of Sirenomelia by Aykut Özek, Mert Turğal, Özgür Özyüncü, Sinan Beksaç

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Antenatal Ultrasound Findings in Fetus with Down Syndrome by Mehmet Serdar KÜTÜK, Mahmut Tuncay ÖZGÜN, Mehmet Dolanbay, Gülsüm Uysal, Aslı Uzak, Elif Kulengir, Semih Uludağ, Mustafa Başbuğ

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Meckel Gruber Syndrome- A Case Report And Review of Literature by Sümeyra Nergiz, Selda Demircan Sezer, Sündüz Özlem Altınkaya, Mert Küçük, Hasan Yüksel

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Cystic Hygroma and Monosomy X by Aykut Özek, Mert Turğal, Özgür Özyüncü, Sinan Beksaç

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Factors Determining Parental Attitudes Towards Termination of Pregnancy in Prenatally Detected Down Syndrome by Ömer Talip Turhan, Mehmet Serdar Kütük, Ruksan Büyükoğlan, Mehmet Dolanbay, Mahmut Tuncay Özgün, Özlem Turhan, Mürşide Şahin

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Abortion Rate Following Chorionic Villous Sampling and Amniocentesis in Twin Pregnancies by Fatemeh Golshahi, Fatemeh Rahimi-Sharbaf, Mahbobeh Shirazi, Sara Saeedi, Athar Abdolrazagh Nejad, Sahar Garfami, Nafise Saedi, Jafar Golshahi, Zeynab Amiriarya, Narjes Tavakolikia, Behrokh Sahebdel

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Evaluation of Associated Structural and Chromosomal Abnormalities in Patients with Fetal Cerebral Ventriculomegaly Detected in Ultrasonographic Imaging by Erkan Cagliyan, Samican Ozmen, Sureyya Saridas Demir, Ceren Aydin, Egehan Bilen, Handan Guleryuz, Elif Yasar, Derya Ercal, Elcin Bora, Tufan Cankaya

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Sporadik İzole Fokomeli by Selda Uysal, Halime Şen Selim, Serenat Eriş, Yakup Yalçın, Çetin Aydın

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Prenatal Counseling and Diagnosis of COX20 Gene-Related Mitochondrial Complex IV Deficiency: A Case Report and Literature Review by Su J, Zeng L, Chen H, Tong J, Chen Y, Huang L, Deng L, Huang Y

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Importance of Aberrant Right Subclavian Artery Detection During Second Trimester Ultrasound Examination in Low-Risk Population by Erdal Seker, Hasan Sut, Mustafa Kocar, Coskun Umit, Esra Ozkavukcu, Acar Koc

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Prenatal ultrasound diagnosis, associated anomalies and pregnancy outcomes of fetal right aortic arch by Yuting Xie, Zongjie Weng, Ronghua Wang, Qiumei Wu, Wen Ling, Jinwen Chen, Shan Guo

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Prenatal Diagnosis of Zellweger Syndrome: Case Report by Bilgin Kütükcü, Meral Topçu, Sinan Beksaç, Ronald J. Wanders

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Evaluation of Fetuses Diagnosed with Megacystis During Prenatal Period by Kemal Sarsmaz, Busra Kanyildiz, Gokcen Orgul, Gokhan Karakoc, Hasan Eroglu, Dilek Sahin, Aykan Yucel

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Family planning and preimplantation testing: family experiences in congenital adrenal hyperplasia by Jessica L. Sandy, Jessica L. Sandy, Jessica L. Sandy, Grant Betts, Jessica L. Harper, Suzanne M. Nevin, Suzanne M. Nevin, Suzanne M. Nevin, Rebecca Deans, Rebecca Deans, Rebecca Deans, Kristen A. Neville, Kristen A. Neville

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Fetal intracranial hemorrhage in second trimester: An ominous finding even after a normal array by Yu-Hong Long, Si-Qi Wu, Xin Wang, Li-Ping Wu, Yi-Min Xiong, Xin Yang, Feng-Xiang Wei

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Prenatal diagnosis of chromothripsis causing complex chromosomal rearrangement involving chromosomes 5, 7 and 11 leading to TWIST1 deletion and Saethre-Chotzen syndrome by Ivana Joksic, Mina Toljic, Nela Maksimovic, Dijana Perovic, Tatjana Damnjanovic, Aleksandar Jurisic

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Genetics in prenatal diagnosis by Karen Mei Xian Lim, Aniza Puteri Mahyuddin, Arundhati Tushar Gosavi, Mahesh Choolani

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Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese families by Bin Mao, Xiaoling Cai, Na Lin, Yulin Jiang, Na Hao, Yifang Dai, Danhua Guo, Deqin He, Huili Xue, Lingji Chen, Qianqian He, Min Zhang, Meihuan Chen, Hailong Huang, Liangpu Xu

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Prenatal diagnosis of mucopolysaccharidosis type I on hepatosplenomegaly and coarse features: a case-report by Maxime Agranier, Florence Demurger, Christele Dubourg, Jerome Fromageot, Anne-Sophie Cabaret Dufour, Erika Launay, Magalie Gournay, Charles Lefèvre, Roseline Froissart, Magali Pettazzoni, Paul Rollier

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Improving prenatal diagnosis with combined karyotyping, CNV-seq and QF-PCR: a comprehensive analysis of chromosomal abnormalities in high-risk pregnancies by Jia-pei Liu, Shan-Bing Wang, Li Luo, Ya-mei Guo

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