The current applications of cell-free fetal DNA in prenatal diagnosis of single-gene diseases: A review by Mohamad Mahdi Mortazavipour, Reza ‎Mahdian, Shirin Shahbazi

Subjects: “…cell-free nucleic acids, prenatal diagnosis, noninvasive prenatal testing, single-gene diseases, non-invasive techniques.…”
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Outcomes of pregnancies with trisomy 16 mosaicism detected by NIPT: a series of case reports by Haishan Peng, Jiexia Yang, Dongmei Wang, Fangfang Guo, Yaping Hou, Aihua Yin

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GenomomFF: Cost-Effective Method to Measure Fetal Fraction by Adaptive Multiple Regression Techniques With Optimally Selected Autosomal Chromosome Regions by Sunshin Kim, Kangseok Kim, Young Joo Jeon

Subjects: “…Non-invasive prenatal testing…”
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Opieka prenatalna nad matką dziecka niepełnosprawnego = Prenatal care for the mother of a disabled child by Lucyna Szefczyk-Polowczyk, Karina Wengel-Woźny, Malwina Respondek, Hanna Pudło

Subjects: “…prenatal tests, mother, pregnancy, disability, badania prenatalne…”
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Le diagnostic prénatal ou un bébé « normal » svp ! by Catherine Rodrigue

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Prenatal diagnosis of mosaic trisomy 2 and literature review by Ting Wang, Jufei Lian, Congmian Ren, Huamei Huang, Yanlin Huang, Ling Xu, Laiping Zheng, Chanhui Cai, Li Guo

Subjects: “…Non-invasive prenatal testing…”
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Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China by Rulin Dai, Yang Yu, Qi Xi, Xiaonan Hu, Haibo Zhu, Ruizhi Liu, Ruixue Wang

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Prenatal cfDNA Screening for Emanuel Syndrome and Other Unbalanced Products of Conception in Carriers of the Recurrent Balanced Translocation t(11;22): One Laboratory’s Retrospecti... by Erica Soster, Brittany Dyr, Samantha Caldwell, Amanda Sussman, Hany Magharyous

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Does a High-Risk (>1/50) Result for First-Trimester Combined Screening Always Entail Invasive Testing? Which Patients from This Group Might Benefit from cfDNA Testing? by Rocío García-Jiménez, Irene Valero, Isabel Corrales-Gutiérrez, Reyes Granell, Carlota Borrero, José Antonio Sainz-Bueno

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A Novel Paradigm for Non-Invasive Prenatal Genetic Screening: Trophoblast Retrieval and Isolation from the Cervix (TRIC) by Kirim Hong, Hee Jin Park, Hee Yeon Jang, Sung Han Shim, Yoon Jang, Soo Hyun Kim, Dong Hyun Cha

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Liquid profiling – circulating nucleic acid diagnostics gains momentum by Holdenrieder Stefan, Klein Hanns-Georg, Winter Christof

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Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome and a normal 46,XX karyotype at birth by Chih-Ping Chen

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A dPCR-NIPT assay for detections of trisomies 21, 18 and 13 in a single-tube reaction-could it replace serum biochemical tests as a primary maternal plasma screening tool? by Peng Dai, Yanfeng Yang, Ganye Zhao, Zhiqiang Gu, Huanan Ren, Shuang Hu, Ning Liu, Weimeng Jiao, Jinfang Li, Xiangdong Kong

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Correlation of Maternal Age, Weight, Pregnancy - associated Plasma Protein A, Free Beta-human Chorionic Gonadotropin, Fetal Crown-rump Length, and Fetal Gender with Fetal DNA Fraction in Non-invasive Prenatal Testing: An Experiment on Iranian Pregnant Women by Milad Dolatkhah, Marjan Rahnamaye Farzami, Ramezan-Ali Khavari-Nejad, Shokoofeh Noori

“…Background: Non-invasive prenatal testing (NIPT) as a novel screening method has been widely proposed to screen for common fetal chromosomal aneuploidies. …”
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Optimization Protocol of Fixation Method for Trophoblast Retrieval from the Cervix (TRIC): A Preliminary Study by Min Jin Lee, Soo Hyun Kim, Sung Han Shim, Hee Yeon Jang, Hee Jin Park, Dong Hyun Cha

Subjects: “…NIPT (noninvasive prenatal testing)…”
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Factors associated with common and atypical chromosome abnormalities after positive combined first-trimester screening in Chinese women: a retrospective cohort study by Annisa Mak, Helena Lee, C. F. Poon, S. L. Kwok, Teresa Ma, K. Y. K. Chan, Anita Kan, Mary Tang, K. Y. Leung

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Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles by Asuka Hori, Hiroko Ogata-Kawata, Aiko Sasaki, Ken Takahashi, Kosuke Taniguchi, Ohsuke Migita, Akihiro Kawashima, Aikou Okamoto, Akihiko Sekizawa, Haruhiko Sago, Fumio Takada, Kazuhiko Nakabayashi, Kenichiro Hata

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Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype by Jieping Song, Wei Jiang, Chengcheng Zhang, Bo Wang

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Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family by Ying Zhang, Juan Chen, Zonghui Feng, Wencheng Li

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Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era by Evy Vervecken, Bettina Blaumeiser, Tina Vanderheyden, Jan Hauspy, Katrien Janssens

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