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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
Prioritization of interventions in pursuit of maternal health policy objectives to mitigate stillbirth risks. An exploratory qualitative study at subnational level in Uganda
Prioritization of interventions in pursuit of maternal health policy objectives to mitigate stillbirth risks. An exploratory qualitative study at subnational level in Uganda
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Prioritization of interventions in pursuit of maternal health policy objectives to mitigate stillbirth risks. An exploratory qualitative study at subnational level in Uganda

BMC health services research, 2021-01, Vol.21 (1), p.53-53, Article 53 [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: 1472-6963 ;EISSN: 1472-6963 ;DOI: 10.1186/s12913-020-06046-z ;PMID: 33430858

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3
Gestational diabetes is associated with the risk of offspring’s congenital anomalies: a register-based cohort study
Gestational diabetes is associated with the risk of offspring’s congenital anomalies: a register-based cohort study
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Gestational diabetes is associated with the risk of offspring’s congenital anomalies: a register-based cohort study

BMC pregnancy and childbirth, 2023-10, Vol.23 (1), p.1-708, Article 708 [Peer Reviewed Journal]

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: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-023-05996-6 ;PMID: 37789251

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4
Gestational age data completeness, quality and validity in population-based surveys: EN-INDEPTH study
Gestational age data completeness, quality and validity in population-based surveys: EN-INDEPTH study
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Gestational age data completeness, quality and validity in population-based surveys: EN-INDEPTH study

Population health metrics, 2021-02, Vol.19 (Suppl 1), p.16-16, Article 16 [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) 2020 ;ISSN: 1478-7954 ;EISSN: 1478-7954 ;DOI: 10.1186/s12963-020-00230-3 ;PMID: 33557866

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5
Post mortem magnetic resonance imaging in the fetus, infant and child: a comparative study with conventional autopsy (MaRIAS Protocol)
Post mortem magnetic resonance imaging in the fetus, infant and child: a comparative study with conventional autopsy (MaRIAS Protocol)
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Post mortem magnetic resonance imaging in the fetus, infant and child: a comparative study with conventional autopsy (MaRIAS Protocol)

BMC pediatrics, 2011-12, Vol.11 (1), p.120-120, Article 120 [Peer Reviewed Journal]

2011 Thayyil 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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2011 Thayyil et al; licensee BioMed Central Ltd. 2011 Thayyil et al; licensee BioMed Central Ltd. ;ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/1471-2431-11-120 ;PMID: 22192497

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6
Sirenomelia associated with an anterior abdominal wall defect: a case report
Sirenomelia associated with an anterior abdominal wall defect: a case report
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Sirenomelia associated with an anterior abdominal wall defect: a case report

Journal of medical case reports, 2019-07, Vol.13 (1), p.213-213, Article 213 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/s13256-019-2162-0 ;PMID: 31300067

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7
Abgrenzung der Totgeburt von der Fehlgeburt – Auswirkungen auf die ärztliche Leichenschau: Eine Auswertung der relevanten Landes- und Bundesgesetze
Abgrenzung der Totgeburt von der Fehlgeburt – Auswirkungen auf die ärztliche Leichenschau: Eine Auswertung der relevanten Landes- und Bundesgesetze
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Abgrenzung der Totgeburt von der Fehlgeburt – Auswirkungen auf die ärztliche Leichenschau: Eine Auswertung der relevanten Landes- und Bundesgesetze

Rechtsmedizin (Berlin, Germany), 2024-02, Vol.34 (1), p.10-16 [Peer Reviewed Journal]

The Author(s) 2023 ;ISSN: 0937-9819 ;EISSN: 1434-5196 ;DOI: 10.1007/s00194-023-00666-5

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8
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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9
Reproductive and obstetric outcomes in mosaic Turner's Syndrome: a cross-sectional study and review of the literature
Reproductive and obstetric outcomes in mosaic Turner's Syndrome: a cross-sectional study and review of the literature
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Reproductive and obstetric outcomes in mosaic Turner's Syndrome: a cross-sectional study and review of the literature

Reproductive biology and endocrinology, 2015-06, Vol.13 (1), p.59-59, Article 59 [Peer Reviewed Journal]

COPYRIGHT 2015 BioMed Central Ltd. ;Doğer et al. 2015 ;ISSN: 1477-7827 ;EISSN: 1477-7827 ;DOI: 10.1186/s12958-015-0055-7 ;PMID: 26060131

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10
Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases
Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases
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Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases

BMC medical genomics, 2021-04, Vol.14 (1), p.106-106, Article 106 [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: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-021-00955-6 ;PMID: 33853619

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11
A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report
A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report
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A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report

Molecular cytogenetics, 2017-09, Vol.10 (1), p.32-6, Article 32 [Peer Reviewed Journal]

COPYRIGHT 2017 BioMed Central Ltd. ;The Author(s). 2017 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-017-0332-6 ;PMID: 28878823

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12
Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients
Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients
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Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients

BMC medical genomics, 2022-04, Vol.15 (1), p.90-90, Article 90 [Peer Reviewed Journal]

2022. The Author(s). ;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: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-022-01240-w ;PMID: 35436901

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13
Performance of noninvasive prenatal testing for twin pregnancies in South China
Performance of noninvasive prenatal testing for twin pregnancies in South China
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Performance of noninvasive prenatal testing for twin pregnancies in South China

Journal of assisted reproduction and genetics, 2023-09, Vol.40 (9), p.2219-2231 [Peer Reviewed Journal]

The Author(s) 2023 ;2023. The Author(s). ;The Author(s) 2023. This work is published 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. ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-023-02881-1 ;PMID: 37480419

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14
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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15
Cell-free fetal DNA testing and its correlation with prenatal indications
Cell-free fetal DNA testing and its correlation with prenatal indications
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Cell-free fetal DNA testing and its correlation with prenatal indications

BMC pregnancy and childbirth, 2021-08, Vol.21 (1), p.585-585, Article 585 [Peer Reviewed Journal]

2021. The Author(s). ;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: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-021-04044-5 ;PMID: 34429082

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16
Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014-2020
Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014-2020
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Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014-2020

Orphanet journal of rare diseases, 2022-12, Vol.17 (1), p.446-446, Article 446 [Peer Reviewed Journal]

2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-022-02594-1 ;PMID: 36550515

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17
Detection rates of abnormalities in over 10,000 amniotic fluid samples at a single laboratory
Detection rates of abnormalities in over 10,000 amniotic fluid samples at a single laboratory
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Detection rates of abnormalities in over 10,000 amniotic fluid samples at a single laboratory

BMC pregnancy and childbirth, 2023-02, Vol.23 (1), p.102-102, Article 102 [Peer Reviewed Journal]

2023. The Author(s). ;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: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-023-05428-5 ;PMID: 36755227

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18
Preconception maternal nutrition: a multi-site randomized controlled trial
Preconception maternal nutrition: a multi-site randomized controlled trial
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Preconception maternal nutrition: a multi-site randomized controlled trial

BMC pregnancy and childbirth, 2014-03, Vol.14 (1), p.111-111, Article 111 [Peer Reviewed Journal]

2014 Hambidge 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/2.0), 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 Hambidge et al.; licensee BioMed Central Ltd. 2014 Hambidge et al.; licensee BioMed Central Ltd. ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/1471-2393-14-111 ;PMID: 24650219

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19
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide
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Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide

Journal of community genetics, 2018-10, Vol.9 (4), p.377-386 [Peer Reviewed Journal]

The Author(s) 2017 ;ISSN: 1868-310X ;EISSN: 1868-6001 ;DOI: 10.1007/s12687-017-0336-2 ;PMID: 28948513

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20
Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral center
Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral center
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Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral center

BMC medicine, 2015-06, Vol.13 (1), p.129-129, Article 129 [Peer Reviewed Journal]

COPYRIGHT 2015 BioMed Central Ltd. ;COPYRIGHT 2015 BioMed Central Ltd. ;Neufeld-Kaiser et al. 2015 ;ISSN: 1741-7015 ;EISSN: 1741-7015 ;DOI: 10.1186/s12916-015-0374-8 ;PMID: 26033224

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