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The Journal of Maternal-Fetal & Neonatal Medicine Volume 12, 2002 - Issue 1
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(RG) Obstetrics and Gynaecology

One-stop clinic for assessment of risk of chromosomal defects at 12 weeks of gestation

K. H. Nicolaides Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, King's College London, London, UK
,
R. Bindra Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, King's College London, London, UK
,
V. Heath Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, King's College London, London, UK
&
S. Cicero Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, King's College London, London, UK
Pages 9-18 | Published online: 07 Jul 2009

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Aleksandra Nikolić, Mirjana Bogavac, Zorica Grujić & Nebojša Kladar. (2022) Disturbance of oxidative balance in the pregnancy with fetal trisomy 21. The Journal of Maternal-Fetal & Neonatal Medicine 35:25, pages 6080-6083.
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Fatma Uysal, Emine Coşar, Kaya Yücesoy, Meryem Gencer, Sibel Cevizci, Ayşenur Güngör, Servet Hacıvelioğlu & Ahmet Uysal. (2015) Is there any relationship between adverse pregnancy outcome and first trimester nuchal translucency measurements in normal karyotype fetuses?. The Journal of Maternal-Fetal & Neonatal Medicine 28:5, pages 531-534.
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Lan-Szu Chou, Elaine Lyon & Rong Mao. (2008) Molecular diagnosis utility of multiplex ligation-dependent probe amplification. Expert Opinion on Medical Diagnostics 2:4, pages 373-385.
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Mark I Evans & Howard S Cuckle. (2007) Biochemical screening for aneuploidy. Expert Review of Obstetrics & Gynecology 2:6, pages 765-773.
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Articles from other publishers (9)

Mark I. Evans & David W. Britt. (2022) Resistance to Change. Reproductive Sciences 30:3, pages 835-853.
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David W. Britt, Shara M. Evans & Mark I. Evans. 2023. Prenatal Diagnostic Testing for Genetic Disorders. Prenatal Diagnostic Testing for Genetic Disorders 79 98 .
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.
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Genevieve Fairbrother, Shayla Johnson, Thomas J. Musci & Ken Song. (2013) Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population. Prenatal Diagnosis 33:6, pages 580-583.
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Amelia L.M. Sutton & Joseph R. Biggio. 2013. Emery and Rimoin's Principles and Practice of Medical Genetics. Emery and Rimoin's Principles and Practice of Medical Genetics 1 23 .
Giovanni Monni, Rosa Maria Ibba & Maria Angelica Zoppi. 2009. Genetic Disorders and the Fetus. Genetic Disorders and the Fetus 160 193 .
Ilan E. Timor-Tritsch. (2006) As Technology Evolves, So Should Its Application. Journal of Ultrasound in Medicine 25:4, pages 423-428.
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Ilan E. Timor-Tritsch, Asher Bashiri, Ana Monteagudo & Alan A. Arslan. (2004) Qualified and trained sonographers in the US can perform early fetal anatomy scans between 11 and 14 weeks. American Journal of Obstetrics and Gynecology 191:4, pages 1247-1252.
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Silvia So-Haei Liu, Mei-Leng Cheong, Jia-Ling Lee, Ming-Song Tsai, Bo-Quing She & Su-Chee Chen. (2004) First-Trimester Combined Test Screening for Down Syndrome: Results of A Series with 5,036 Cases. Taiwanese Journal of Obstetrics and Gynecology 43:2, pages 72-76.
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