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1
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
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Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

PloS one, 2016-08, Vol.11 (8), p.e0161045-e0161045 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Samango-Sprouse 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. ;2016 Samango-Sprouse et al 2016 Samango-Sprouse et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0161045 ;PMID: 27512996

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2
Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing
Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing
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Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing

Clinical chemistry (Baltimore, Md.), 2014-01, Vol.60 (1), p.251-259 [Peer Reviewed Journal]

COPYRIGHT 2014 American Association for Clinical Chemistry, Inc. ;Copyright American Association for Clinical Chemistry Jan 2014 ;ISSN: 0009-9147 ;EISSN: 1530-8561 ;DOI: 10.1373/clinchem.2013.215145 ;PMID: 24193117

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3
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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4
Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies
Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies
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Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1654-n/a [Peer Reviewed Journal]

2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1654 ;PMID: 33755350

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5
Retrieval of Trophoblast Cells from the Cervical Canal: A Promising Non-invasive Method for Prenatal Diagnosis
Retrieval of Trophoblast Cells from the Cervical Canal: A Promising Non-invasive Method for Prenatal Diagnosis
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Retrieval of Trophoblast Cells from the Cervical Canal: A Promising Non-invasive Method for Prenatal Diagnosis

Alternative therapies in health and medicine, 2023-10, Vol.29 (7), p.444-446 [Peer Reviewed Journal]

Copyright InnoVision Health Media, Inc. Oct 2023 ;ISSN: 1078-6791 ;PMID: 37535925

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6
Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication
Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication
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Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication

European journal of medical research, 2023-08, Vol.28 (1), p.1-304, Article 304 [Peer Reviewed Journal]

COPYRIGHT 2023 BioMed Central Ltd. ;2023. 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. ;BioMed Central Ltd., part of Springer Nature 2023 ;ISSN: 2047-783X ;ISSN: 0949-2321 ;EISSN: 2047-783X ;DOI: 10.1186/s40001-023-01285-2 ;PMID: 37644576

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7
Clinical application of noninvasive prenatal testing in the detection of fetal chromosomal diseases
Clinical application of noninvasive prenatal testing in the detection of fetal chromosomal diseases
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Clinical application of noninvasive prenatal testing in the detection of fetal chromosomal diseases

Molecular cytogenetics, 2021-06, Vol.14 (1), p.1-31, Article 31 [Peer Reviewed Journal]

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: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-021-00550-5 ;PMID: 34127051

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8
High accuracy of quantitative fluorescence polymerase chain reaction combined with non-invasive pre-natal testing for mid-pregnancy diagnosis of common fetal aneuploidies: A single-center experience in China
High accuracy of quantitative fluorescence polymerase chain reaction combined with non-invasive pre-natal testing for mid-pregnancy diagnosis of common fetal aneuploidies: A single-center experience in China
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High accuracy of quantitative fluorescence polymerase chain reaction combined with non-invasive pre-natal testing for mid-pregnancy diagnosis of common fetal aneuploidies: A single-center experience in China

Experimental and therapeutic medicine, 2019-07, Vol.18 (1), p.711-721

COPYRIGHT 2019 Spandidos Publications ;Copyright Spandidos Publications UK Ltd. 2019 ;Copyright © 2019, Spandidos Publications 2019 ;ISSN: 1792-0981 ;EISSN: 1792-1015 ;DOI: 10.3892/etm.2019.7625 ;PMID: 31281451

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9
Second-generation non-invasive high-throughput DNA sequencing technology in the screening of Down's syndrome in advanced maternal age women
Second-generation non-invasive high-throughput DNA sequencing technology in the screening of Down's syndrome in advanced maternal age women
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Second-generation non-invasive high-throughput DNA sequencing technology in the screening of Down's syndrome in advanced maternal age women

Biomedical reports, 2016-06, Vol.4 (6), p.715-718

COPYRIGHT 2016 Spandidos Publications ;Copyright Spandidos Publications UK Ltd. 2016 ;Copyright © 2016, Spandidos Publications 2016 ;ISSN: 2049-9434 ;EISSN: 2049-9442 ;DOI: 10.3892/br.2016.653 ;PMID: 27313855

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10
Impact of abnormal karyotype on reproductive outcome in premature ovarian insufficiency
Impact of abnormal karyotype on reproductive outcome in premature ovarian insufficiency
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Impact of abnormal karyotype on reproductive outcome in premature ovarian insufficiency

Reproductive medicine and biology, 2022-01, Vol.21 (1), p.e12471-n/a [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine ;2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1445-5781 ;EISSN: 1447-0578 ;DOI: 10.1002/rmb2.12471 ;PMID: 35755970

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11
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses
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Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses

European journal of human genetics : EJHG, 2009-07, Vol.17 (7), p.897-903 [Peer Reviewed Journal]

2009 INIST-CNRS ;Copyright Nature Publishing Group Jul 2009 ;Copyright © 2009 Macmillan Publishers Limited 2009 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2008.265 ;PMID: 19156167

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12
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain
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Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain

Genes, 2024-05, Vol.15 (5), p.568 [Peer Reviewed Journal]

COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes15050568 ;PMID: 38790198

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13
Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth
Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth
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Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth

Molecular genetics & genomic medicine, 2023-08, Vol.11 (8), p.e2187-n/a [Peer Reviewed Journal]

2023 The Authors. published by Wiley Periodicals LLC. ;2023 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2023. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.2187 ;PMID: 37073418

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14
Optimal Detection of Fetal Chromosomal Abnormalities by Massively Parallel DNA Sequencing of Cell-Free Fetal DNA from Maternal Blood
Optimal Detection of Fetal Chromosomal Abnormalities by Massively Parallel DNA Sequencing of Cell-Free Fetal DNA from Maternal Blood
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Optimal Detection of Fetal Chromosomal Abnormalities by Massively Parallel DNA Sequencing of Cell-Free Fetal DNA from Maternal Blood

Clinical chemistry (Baltimore, Md.), 2011-07, Vol.57 (7), p.1042-1049 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 American Association for Clinical Chemistry, Inc. ;Copyright American Association for Clinical Chemistry Jul 2011 ;ISSN: 0009-9147 ;EISSN: 1530-8561 ;DOI: 10.1373/clinchem.2011.165910 ;PMID: 21519036 ;CODEN: CLCHAU

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15
Performance of cell-free DNA sequencing-based non-invasive prenatal testing: experience on 36,456 singleton and multiple pregnancies
Performance of cell-free DNA sequencing-based non-invasive prenatal testing: experience on 36,456 singleton and multiple pregnancies
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Performance of cell-free DNA sequencing-based non-invasive prenatal testing: experience on 36,456 singleton and multiple pregnancies

BMC medical genomics, 2021-03, Vol.14 (1), p.93-93, Article 93 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;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/s12920-021-00941-y ;PMID: 33785045

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16
Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road?
Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road?
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Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road?

Clinical chemistry (Baltimore, Md.), 2014-01, Vol.60 (1), p.78-87 [Peer Reviewed Journal]

COPYRIGHT 2014 American Association for Clinical Chemistry, Inc. ;Copyright American Association for Clinical Chemistry Jan 2014 ;ISSN: 0009-9147 ;EISSN: 1530-8561 ;DOI: 10.1373/clinchem.2013.202663 ;PMID: 24255077

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17
Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China
Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China
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Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China

Genes, 2021-03, Vol.12 (4), p.478 [Peer Reviewed Journal]

2021 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 (http://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. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12040478 ;PMID: 33806256

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18
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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19
Clinical Potential of Expanded Noninvasive Prenatal Testing for Detection of Aneuploidies and Microdeletion/Microduplication Syndromes
Clinical Potential of Expanded Noninvasive Prenatal Testing for Detection of Aneuploidies and Microdeletion/Microduplication Syndromes
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Clinical Potential of Expanded Noninvasive Prenatal Testing for Detection of Aneuploidies and Microdeletion/Microduplication Syndromes

Molecular diagnosis & therapy, 2023-11, Vol.27 (6), p.769-779

The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG. ;Copyright Springer Nature B.V. Nov 2023 ;ISSN: 1177-1062 ;EISSN: 1179-2000 ;DOI: 10.1007/s40291-023-00674-x ;PMID: 37689607

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Citations Cited by
20
The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis
The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis
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The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis

Journal of clinical laboratory analysis, 2020-12, Vol.34 (12), p.e23514-n/a [Peer Reviewed Journal]

2020 The Authors. Published by Wiley Periodicals LLC ;2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals LLC. ;2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.23514 ;PMID: 32864771

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