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The Journal of Maternal-Fetal & Neonatal Medicine Volume 25, 2012 - Issue 12
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Original Article

Non-invasive prenatal screening of fetal sex chromosomal abnormalities: perspective of pregnant women

Tze Kin LauFetal Medicine Centre, Paramount Clinic, Central, Hong KongCorrespondence[email protected]
,
Mei Ki ChanBGI-Shenzhen, Shenzhen, China
,
Pui Shan Salome LoFetal Medicine Centre, Paramount Clinic, Central, Hong Kong
,
Hon Yee Connie ChanFetal Medicine Centre, Paramount Clinic, Central, Hong Kong
,
WaiSze Kim ChanFetal Medicine Centre, Paramount Clinic, Central, Hong Kong
,
Tik Yee KooFetal Medicine Centre, Paramount Clinic, Central, Hong Kong
,
Hoi Yan Joyce NgFetal Medicine Centre, Paramount Clinic, Central, Hong Kong
&
Ritsuko K. PoohCRIFM Clinical Research Institute of Fetal Medicine PMC, Osaka, Japan
 show all
Pages 2616-2619 | Received 14 Apr 2012, Accepted 26 Jun 2012, Published online: 10 Aug 2012

Citations (24)

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Cechuan Deng, Sau Wai Cheung & Hongqian Liu. (2021) Noninvasive prenatal screening for fetal sex chromosome aneuploidies. Expert Review of Molecular Diagnostics 21:4, pages 405-415.
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Herb Brar, Eric Wang, Craig Struble, Thomas J. Musci & Mary E. Norton. (2013) The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy. The Journal of Maternal-Fetal & Neonatal Medicine 26:2, pages 143-145.
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Articles from other publishers (22)

Sofia Bussolaro, Yvette C. Raymond, Melissa L. Acreman, Maurizio Guido, Fabricio Da Silva Costa, Daniel L. Rolnik & Ilaria Fantasia. (2023) The accuracy of prenatal cell-free DNA screening for sex chromosome abnormalities: A systematic review and meta-analysis. American Journal of Obstetrics & Gynecology MFM 5:3, pages 100844.
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Jane Fisher & Hannah McInnes‐Dean. (2022) When a sex chromosome aneuploidy is diagnosed—views from a parent support organisation. Prenatal Diagnosis 43:2, pages 235-239.
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Molly Johnston, Chanelle Warton, Mark D. Pertile, Michelle Taylor‐Sands, Martin B. Delatycki, Lisa Hui, Julian Savulescu & Catherine Mills. (2022) Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy. Prenatal Diagnosis 43:2, pages 226-234.
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Maaged A. Akiel, Mohamud S. Mohamud, Emad M. Masuadi & Hassan S. Alamri. (2022) Knowledge and attitude of pregnant women in the Kingdom of Saudi Arabia toward Noninvasive prenatal testing: A single center study. Molecular Genetics & Genomic Medicine 10:7.
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Gareth M. ThomasBarbara Katz RothmanHeather StrangeJoanna E. Latimer. (2020) Testing Times: The Social Life of Non-invasive Prenatal Testing. Science, Technology and Society 26:1, pages 81-97.
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Jia-Zhen Chang, Qing-Wei Qi, Xi-Ya Zhou, Yu-Lin Jiang, Na Hao & Jun-Tao Liu. (2020) Noninvasive Prenatal Testing for Fetal XXY Aneuploidies Among Pregnancies in Beijing of China. Maternal-Fetal Medicine 2:4, pages 199-206.
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A. Kater-Kuipers, E. M. Bunnik, I. D. de Beaufort & R. J. H. Galjaard. (2018) Limits to the scope of non-invasive prenatal testing (NIPT): an analysis of the international ethical framework for prenatal screening and an interview study with Dutch professionals. BMC Pregnancy and Childbirth 18:1.
Crossref
Allanah Howard‐Bath, Alice Poulton, Jane Halliday & Lisa Hui. (2018) Population‐based trends in the prenatal diagnosis of sex chromosome aneuploidy before and after non‐invasive prenatal testing. Prenatal Diagnosis 38:13, pages 1062-1068.
Crossref
T.K. Lau. 2018. Dewhurst's Textbook of Obstetrics & Gynaecology. Dewhurst's Textbook of Obstetrics & Gynaecology 58 70 .
Po Lam So, Kwun Yue Yvonne Cheng, Kwan Yiu Cheuk, Wan Kam Chiu, Shui Lam Mak, Sau Lan Mok, Tsz Kin Lo, Wai Kuen Yung, Fai Man Lo, Hon Yin Brian Chung, Sik Yau Anita Kan, Chin Peng Lee & Hoi Yin Mary Tang. (2017) Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong. Journal of Obstetrics and Gynaecology Research 43:12, pages 1821-1829.
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Alison DeMaio, Andrew Green & Sean Daly. (2016) Maternal 47,XX,i(X)(q10) as a cause of false positive sex chromosome aneuploidy in noninvasive prenatal screening. Prenatal Diagnosis 36:7, pages 693-695.
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Melissa Hill, Celine Lewis & Lyn S. Chitty. (2016) Stakeholder attitudes and needs regarding cell-free fetal DNA testing. Current Opinion in Obstetrics & Gynecology 28:2, pages 125-131.
Crossref
Sung-Hee Han, Young-Ho Yang, Jae-Song Ryu, Myung-Soo Kang, Young-Jin Kim & Kyoung-Ryul Lee. (2015) Noninvasive prenatal test for fetal chromosomal aneuploidies by massively parallel sequencing of cell-free fetal DNA in maternal plasma: The first clinical experience in Korea. Journal of Genetic Medicine 12:2, pages 85-91.
Crossref
Ruth M. Farrell, Patricia K. Agatisa, MaryBeth Mercer & Marissa B. Coleridge. (2015) Online direct-to-consumer messages about non-invasive prenatal genetic testing. Reproductive Biomedicine & Society Online 1:2, pages 88-97.
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Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall, Lidewij Henneman, Heidi C Howard, Anneke Lucassen, Kelly Ormond, Borut Peterlin, Dragica Radojkovic, Wolf Rogowski, Maria Soller, Aad Tibben, Lisbeth Tranebjærg, Carla G van El & Martina C Cornel. (2015) Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. European Journal of Human Genetics 23:11, pages 1438-1450.
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Patricia K. Agatisa, Mary Beth Mercer, Angela C. Leek, Marissa B. Smith, Elliot Philipson & Ruth M. Farrell. (2015) A first look at women's perspectives on noninvasive prenatal testing to detect sex chromosome aneuploidies and microdeletion syndromes. Prenatal Diagnosis 35:7, pages 692-698.
Crossref
L. Hui, M. Teoh, F. da Silva Costa, P. Ramsay, R. Palma‐Dias, Z. Richmond, S. Piessens & S. Walker. (2015) Clinical implementation of cell‐free DNA ‐based aneuploidy screening: perspectives from a national audit . Ultrasound in Obstetrics & Gynecology 45:1, pages 10-15.
Crossref
SUZANNE DRURY, MELISSA HILL & LYN S CHITTY. (2016) RECENT DEVELOPMENTS IN NON-INVASIVE PRENATAL DIAGNOSIS AND TESTING. Fetal and Maternal Medicine Review 25:3-4, pages 295-317.
Crossref
H. Yao, F. Jiang, H. Hu, Y. Gao, Z. Zhu, H. Zhang, Y. Wang, Y. Guo, L. Liu, Y. Yuan, L. Zhou, J. Wang, B. Du, N. Qu, R. Zhang, Y. Dong, H. Xu, F. Chen, H. Jiang, Y. Liu, L. Zhang, Z. Tian, Q. Liu, C. Zhang, X. Pan, S. Yang, L. Zhao, W. Wang & Z. Liang. (2014) Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital. Ultrasound in Obstetrics & Gynecology 44:1, pages 17-24.
Crossref
T. K. Lau, S. W. Cheung, P. S. S. Lo, A. N. Pursley, M. K. Chan, F. Jiang, H. Zhang, W. Wang, L. F. J. Jong, O. K. C. Yuen, H. Y. C. Chan, W. S. K. Chan & K. W. Choy. (2014) Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. Ultrasound in Obstetrics & Gynecology 43:3, pages 254-264.
Crossref
Huso Yi, Nina Hallowell, Sian Griffiths & Tak Yeung Leung. (2013) Motivations for Undertaking DNA Sequencing-Based Non-Invasive Prenatal Testing for Fetal Aneuploidy: A Qualitative Study with Early Adopter Patients in Hong Kong. PLoS ONE 8:11, pages e81794.
Crossref
Lisa Hui & Diana W. Bianchi. (2013) Recent advances in the prenatal interrogation of the human fetal genome. Trends in Genetics 29:2, pages 84-91.
Crossref

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