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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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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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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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 Cytogenetic Findings in 13.466 Cases of High-Risk Pregnant Women in One Laboratory by Leyla Özer, Evrim Ünsal, Özge Ayvaz, Aşkın Şen, Volkan Baltacı

Subjects: “…Prenatal diagnosis…”
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Noninvasive prenatal diagnosis (NIPD) of non-syndromic hearing loss (NSHL) for singleton and twin pregnancies in the first trimester by Huanyun Li, Shaojun Li, Zhenhua Zhao, Lingrong Kong, Xinyu Fu, Jingqi Zhu, Jun Feng, Weiqin Tang, Di Wu, Xiangdong Kong

Subjects: “…Noninvasive prenatal diagnosis…”
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Prenatal Detection of Silver–Russell Syndrome: A First Trimester Suspicion and Diagnostic Approach by Slavyana Galeva, Giuliana Diglio, Boris Stoilov, Ekaterina Uchikova, Lucian Pop

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Fetal Bradyarrhythmias: A Comprehensive Update on Current Knowledge by Maria Elisa Martini Albrecht, Larissa Keren de Azevedo Teixeira, Edward Araujo Júnior, Nathalie Jeanne Bravo-Valenzuela, Roberta Granese

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Analysis of prenatal diagnosis and pregnancy outcomes for rare autosomal trisomies detected by non-invasive prenatal testing in 33,079 cases by Xu Yan, Kai Ding, Xin Zhang, Shuai Zhang, Haiying Peng, Ying Zhang

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Prenatally Diagnosed Cardiac Tumors and Tuberous Sclerosis Complex: A Single-Center Experience by Matija Bakoš, Dora Jelinek, Ana Ćorić Ljoka, Nada Sindičić Dessardo, Dalibor Šarić, Ruža Grizelj

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Unraveling the genetic mysteries of spinal muscular atrophy in Chinese families by Shanshan Gao, Duo Chen, Qianqian Li, Xuechao Zhao, Chen Chen, Lina Liu, Miao Jiang, Zhenhua Zhao, Yanhua Wang, Xiangdong Kong

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