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Hua-Pin Chang, Jeng-Yuan Chiou, Jia-Yuh Chen & Pen-Hua Su. (2017) Prenatal cytogenetic diagnosis in Taiwan: a nationwide population-based study. The Journal of Maternal-Fetal & Neonatal Medicine 30:21, pages 2521-2528.
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Articles from other publishers (14)
Ci Pan, Zilong Li, Guomei Cheng, Xiaohua Luo, Fufang Nie, Jing GaoPeifeng Yang. (2023) Association between chromosome abnormities and prenatal diagnosis indicators screening in the second trimester of pregnancy. Medicine 102:35, pages e34762.
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Meiying Cai, Na Lin, Xuemei Chen, Ying Li, Min Lin, Xianguo Fu, Hailong Huang, Shuqiong He & Liangpu Xu. (2023) Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China. Brazilian Journal of Medical and Biological Research 56.
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Salim Sezer, Melih Bestel, Gökhan Bolluk & Alper Gezdirici. (2022) The Importance of Screening Tests and Amniocentesis in Approach to Pregnant Women Over the Age of Thirty-Five. Journal of Academic Research in Medicine 12:3, pages 155-158.
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Lin Chen, Li Wang, Daishu Yin, Feng Tang, Yang Zeng, Hongmei Zhu & Jing Wang. (2022) Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities. BMC Genomics 23:1.
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Cong Zhang, Liying Yan & Jie Qiao. (2022) Effect of advanced parental age on pregnancy outcome and offspring health. Journal of Assisted Reproduction and Genetics 39:9, pages 1969-1986.
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Shimin Yuan, Liuliang Guo, Dehua Cheng, Xiurong Li, Hao Hu, Liang Hu, Guangxiu Lu, Ge Lin, Fei Gong & Yue-Qiu Tan. (2022) The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception. Journal of Assisted Reproduction and Genetics 39:7, pages 1683-1689.
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Hilmi BOLAT & Gül ÜNSEL-BOLAT. (2021) Down Sendromu Tanılı Olgularda Aile ve Çocuğa Ait Sosyodemografik Özelliklerin Değerlendirilmesi. Balıkesır Health Sciences Journal.
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Hongge Li, Yuchan Mao & Jinglei Jin. (2021) The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China. Molecular Cytogenetics 14:1.
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Sarang Younesi, Mohammad Mahdi Taheri Amin, Sedigheh Hantoushzadeh, Pourandokht Saadati, Soudabeh Jamali, Mohammad-Hossein Modarressi, Shahram Savad, Saeed Delshad, Saloomeh Amidi, Taraneh Geranorimi, Fariba Navidpour & Soudeh Ghafouri-Fard. (2021) Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women. Scientific Reports 11:1.
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Suping Li, Yuxia Jin, Jing Yang, Li Yang, Ping Tang, Chiyan Zhou, Liping Wu, Jinhua Dong, Jie Chen & Huaxiang Shen. (2020) Prenatal diagnosis of rearrangements in the fetal 22q11.2 region. Molecular Cytogenetics 13:1.
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Julia Bijok, Anna Kucińska–Chahwan, Diana Massalska, Alicja Ilnicka, Grzegorz Panek & Tomasz Roszkowski. (2020) In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland. Journal of Assisted Reproduction and Genetics 37:8, pages 1999-2006.
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Huan Huang, You Zhou, Jiajia Zhang, Weiyin Yao & Guoying Zhang. (2019) Prenatal diagnosis of genetic diseases directly using paper-dried cord blood as the starting material for PCR. Analytical and Bioanalytical Chemistry 411:26, pages 6825-6835.
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Xiang Liu, Yijun Song, Zhengguang Guo, Wei Sun & Juntao Liu. (2019) A comprehensive profile and inter-individual variations analysis of the human normal amniotic fluid proteome. Journal of Proteomics 192, pages 1-9.
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Shuo Zhang, Caixia Lei, Junping Wu, Haiyan Sun, Yuezhou Yang, Yueping Zhang & Xiaoxi Sun. (2017) A Retrospective Study of Cytogenetic Results From Amniotic Fluid in 5328 Fetuses With Abnormal Obstetric Sonographic Findings. Journal of Ultrasound in Medicine 36:9, pages 1809-1817.
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