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1
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases
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Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases

Molecular cytogenetics, 2021-01, Vol.14 (1), p.1-1, Article 1 [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/s13039-020-00521-2 ;PMID: 33407708

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2
The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China
The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China
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The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China

Molecular cytogenetics, 2021-05, Vol.14 (1), p.25-25, Article 25 [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/s13039-021-00545-2 ;PMID: 33971935

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3
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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4
Cell-free DNA screening for sex chromosome aneuploidies by non-invasive prenatal testing in maternal plasma
Cell-free DNA screening for sex chromosome aneuploidies by non-invasive prenatal testing in maternal plasma
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Cell-free DNA screening for sex chromosome aneuploidies by non-invasive prenatal testing in maternal plasma

Molecular cytogenetics, 2020-03, Vol.13 (1), p.10-10, Article 10 [Peer Reviewed Journal]

The Author(s). 2020. ;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: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-020-0478-5 ;PMID: 32190123

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5
Positive predictive value estimates for noninvasive prenatal testing from data of a prenatal diagnosis laboratory and literature review
Positive predictive value estimates for noninvasive prenatal testing from data of a prenatal diagnosis laboratory and literature review
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Positive predictive value estimates for noninvasive prenatal testing from data of a prenatal diagnosis laboratory and literature review

Molecular cytogenetics, 2022-07, Vol.15 (1), p.1-29, Article 29 [Peer Reviewed Journal]

COPYRIGHT 2022 BioMed Central Ltd. ;2022. 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) 2022 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-022-00607-z ;PMID: 35794576

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6
Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test
Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test
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Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test

Molecular cytogenetics, 2019-07, Vol.12 (1), p.34-34, Article 34 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;2019. 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). 2019 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-019-0446-0 ;PMID: 31338126

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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
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray
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Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray

Molecular cytogenetics, 2023-06, Vol.16 (1), p.10-10, Article 10 [Peer Reviewed Journal]

2023. The Author(s). ;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. ;The Author(s) 2023 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-023-00642-4 ;PMID: 37301962

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9
Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies
Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies
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Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies

Molecular cytogenetics, 2019-06, Vol.12 (1), p.29-29, Article 29 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-019-0441-5 ;PMID: 31249627

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10
Performance of non-invasive prenatal testing for foetal chromosomal abnormalities in 1048 twin pregnancies
Performance of non-invasive prenatal testing for foetal chromosomal abnormalities in 1048 twin pregnancies
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Performance of non-invasive prenatal testing for foetal chromosomal abnormalities in 1048 twin pregnancies

Molecular cytogenetics, 2021-06, Vol.14 (1), p.1-32, Article 32 [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/s13039-021-00551-4 ;PMID: 34193223

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11
Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency
Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency
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Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Molecular cytogenetics, 2023-09, Vol.16 (1), p.1-22, Article 22 [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: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-023-00650-4 ;PMID: 37660152

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12
Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China
Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China
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Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China

Molecular cytogenetics, 2023-02, Vol.16 (1), p.3-3, Article 3 [Peer Reviewed Journal]

2023. The Author(s). ;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. ;The Author(s) 2023 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-022-00633-x ;PMID: 36765363

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13
Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China
Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China
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Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China

Molecular cytogenetics, 2019-11, Vol.12 (1), p.45-45, Article 45 [Peer Reviewed Journal]

The Author(s). 2019. ;COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-019-0457-x ;PMID: 31709014

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14
Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT
Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT
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Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT

Molecular cytogenetics, 2016-09, Vol.9 (1), p.69-69, Article 69 [Peer Reviewed Journal]

COPYRIGHT 2016 BioMed Central Ltd. ;Copyright BioMed Central 2016 ;The Author(s). 2016 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-016-0279-z ;PMID: 27610202

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15
A prenatal case with discrepant findings between non-invasive prenatal testing and fetal genetic testings
A prenatal case with discrepant findings between non-invasive prenatal testing and fetal genetic testings
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A prenatal case with discrepant findings between non-invasive prenatal testing and fetal genetic testings

Molecular cytogenetics, 2014-07, Vol.7 (1), p.48-48, Article 48 [Peer Reviewed Journal]

COPYRIGHT 2014 BioMed Central Ltd. ;2014 Pan et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. ;Copyright © 2014 Pan et al.; licensee BioMed Central Ltd. 2014 Pan et al.; licensee BioMed Central Ltd. ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/1755-8166-7-48 ;PMID: 25478006

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16
Trisomy Xp and partial tetrasomy Xq resulting from gain of a rearranged X chromosome in a female fetus: pathogenic or not?
Trisomy Xp and partial tetrasomy Xq resulting from gain of a rearranged X chromosome in a female fetus: pathogenic or not?
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Trisomy Xp and partial tetrasomy Xq resulting from gain of a rearranged X chromosome in a female fetus: pathogenic or not?

Molecular cytogenetics, 2015-07, Vol.8 (1), p.53, Article 53 [Peer Reviewed Journal]

COPYRIGHT 2015 BioMed Central Ltd. ;Copyright BioMed Central 2015 ;Yiu et al. 2015 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-015-0160-5 ;PMID: 26213575

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