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1
A case of placental trisomy 18 mosaicism causing a false negative NIPT result
A case of placental trisomy 18 mosaicism causing a false negative NIPT result
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A case of placental trisomy 18 mosaicism causing a false negative NIPT result

Molecular cytogenetics, 2017-10, Vol.10 (1), p.40-4, Article 40 [Peer Reviewed Journal]

COPYRIGHT 2017 BioMed Central Ltd. ;Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-017-0341-5 ;PMID: 29093756

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2
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
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Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience

BMC research notes, 2020-03, Vol.13 (1), p.167-167, Article 167 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1756-0500 ;EISSN: 1756-0500 ;DOI: 10.1186/s13104-020-05009-1 ;PMID: 32188487

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3
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
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Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center

Molecular cytogenetics, 2021-12, Vol.14 (1), p.1-56, Article 56 [Peer Reviewed Journal]

2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-021-00577-8 ;PMID: 34863241

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4
Detection of chromosomal abnormalities, congenital abnormalities and transfusion syndrome in twins
Detection of chromosomal abnormalities, congenital abnormalities and transfusion syndrome in twins
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Detection of chromosomal abnormalities, congenital abnormalities and transfusion syndrome in twins

Ultrasound in obstetrics & gynecology, 2007-05, Vol.29 (5), p.517 [Peer Reviewed Journal]

Copyright (c) 2007 ISUOG. ;ISSN: 0960-7692 ;EISSN: 1469-0705 ;DOI: 10.1002/uog.3918 ;PMID: 17429797

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5
Efficacy of metamizole versus ibuprofen and a short educational intervention versus standard care in acute and subacute low back pain: a study protocol of a randomised, multicentre, factorial trial (EMISI trial)
Efficacy of metamizole versus ibuprofen and a short educational intervention versus standard care in acute and subacute low back pain: a study protocol of a randomised, multicentre, factorial trial (EMISI trial)
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Efficacy of metamizole versus ibuprofen and a short educational intervention versus standard care in acute and subacute low back pain: a study protocol of a randomised, multicentre, factorial trial (EMISI trial)

BMJ open, 2021-10, Vol.11 (10), p.e048531-e048531 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. 2021 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2020-048531 ;PMID: 34645660

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6
Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations
Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations
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Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations

BMC medical genomics, 2021-12, Vol.14 (1), p.292-292, Article 292 [Peer Reviewed Journal]

2021. The Author(s). ;COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-021-01131-6 ;PMID: 34895207

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7
Miscarriage after a normal scan at 12-14 gestational weeks in women at low risk of carrying a fetus with chromosomal anomaly according to nuchal translucency screening
Miscarriage after a normal scan at 12-14 gestational weeks in women at low risk of carrying a fetus with chromosomal anomaly according to nuchal translucency screening
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Miscarriage after a normal scan at 12-14 gestational weeks in women at low risk of carrying a fetus with chromosomal anomaly according to nuchal translucency screening

Ultrasound in obstetrics & gynecology, 2007-10, Vol.30 (5), p.728 [Peer Reviewed Journal]

Copyright (c) 2007 ISUOG ;ISSN: 0960-7692 ;ISSN: 1469-0705 ;EISSN: 1469-0705 ;DOI: 10.1002/uog.5138 ;PMID: 17823976

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8
Non-Invasive Prenatal Testing beyond Trisomies
Non-Invasive Prenatal Testing beyond Trisomies
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Non-Invasive Prenatal Testing beyond Trisomies

Journal of medicine and life, 2019-07, Vol.12 (3), p.221-224

Carol Davila University Press. ;Copyright Carol Daila University Foundation Jul-Sep 2019 ;Carol Davila University Press 2019 ;ISSN: 1844-122X ;EISSN: 1844-3117 ;DOI: 10.25122/jml-2019-0053 ;PMID: 31666820

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9
Non-invasive prenatal testing: ethical issues explored
Non-invasive prenatal testing: ethical issues explored
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Non-invasive prenatal testing: ethical issues explored

European journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.272-277 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Mar 2010 ;Copyright © 2010 Macmillan Publishers Limited 2010 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2009.203 ;PMID: 19953123

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10
Obstetric Outcomes in Women with Turner Karyotype
Obstetric Outcomes in Women with Turner Karyotype
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Obstetric Outcomes in Women with Turner Karyotype

The journal of clinical endocrinology and metabolism, 2011-11, Vol.96 (11), p.3475-3482 [Peer Reviewed Journal]

Copyright © 2011 by The Endocrine Society ;2015 INIST-CNRS ;ISSN: 0021-972X ;ISSN: 1945-7197 ;EISSN: 1945-7197 ;DOI: 10.1210/jc.2011-1421 ;PMID: 21865365 ;CODEN: JCEMAZ

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11
Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations
Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations
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Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations

The Journal of clinical investigation, 2015-10, Vol.125 (10), p.3757-3765 [Peer Reviewed Journal]

COPYRIGHT 2015 American Society for Clinical Investigation ;COPYRIGHT 2015 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Oct 2015 ;Copyright © 2015, American Society for Clinical Investigation 2015 American Society for Clinical Investigation ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI79322 ;PMID: 26426075

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12
Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis
Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis
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Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis

PloS one, 2017-02, Vol.12 (2), p.e0171886-e0171886 [Peer Reviewed Journal]

COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 Lou et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017 Lou et al 2017 Lou et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0171886 ;PMID: 28241016

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13
Reproductive Outcomes of Women with Turner Syndrome Undergoing Oocyte Vitrification: A Retrospective Multicenter Cohort Study
Reproductive Outcomes of Women with Turner Syndrome Undergoing Oocyte Vitrification: A Retrospective Multicenter Cohort Study
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Reproductive Outcomes of Women with Turner Syndrome Undergoing Oocyte Vitrification: A Retrospective Multicenter Cohort Study

Journal of clinical medicine, 2023-10, Vol.12 (20), p.6502 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm12206502 ;PMID: 37892640

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14
The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies
The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies
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The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies

Molecular cytogenetics, 2018-12, Vol.11 (1), p.59-59, Article 59 [Peer Reviewed Journal]

COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s). 2018 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-018-0407-z ;PMID: 30524505

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