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1
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1279 ;PMID: 32463164

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2
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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3
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence
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Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence

Molecular genetics & genomic medicine, 2020-07, Vol.8 (7), p.e1297-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1297 ;PMID: 32383339

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4
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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5
National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017
National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017
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National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017

Acta obstetricia et gynecologica Scandinavica, 2021-05, Vol.100 (5), p.884-892 [Peer Reviewed Journal]

2021 Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). Published by John Wiley & Sons Ltd ;2021 Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). Published by John Wiley & Sons Ltd. ;COPYRIGHT 2021 Wiley Subscription Services, Inc. ;Copyright © 2021 Acta Obstetricia et Gynecologica Scandinavica ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14052 ;PMID: 33230826

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6
Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing
Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing
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Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing

The journal of gene medicine, 2021-05, Vol.23 (5), p.e3324-n/a [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Ltd. ;2021 The Authors. The Journal of Gene Medicine published by John Wiley & Sons Ltd. ;COPYRIGHT 2021 Wiley Subscription Services, Inc. ;2021. This article 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: 1099-498X ;EISSN: 1521-2254 ;DOI: 10.1002/jgm.3324 ;PMID: 33615614

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7
Evaluation of the clinical effects of non-invasive prenatal screening for diseases associated with aneuploidy and copy number variation
Evaluation of the clinical effects of non-invasive prenatal screening for diseases associated with aneuploidy and copy number variation
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Evaluation of the clinical effects of non-invasive prenatal screening for diseases associated with aneuploidy and copy number variation

Molecular genetics & genomic medicine, 2023-09, Vol.11 (9), p.e2200-e2200 [Peer Reviewed Journal]

2023 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;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. ;2023 The Authors. published by Wiley Periodicals LLC. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.2200 ;PMID: 37354111

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8
Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China
Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China
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Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China

Molecular genetics & genomic medicine, 2020-10, Vol.8 (10), p.e1446-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC. ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1446 ;PMID: 32767744

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9
Prenatal cell‐free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory
Prenatal cell‐free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory
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Prenatal cell‐free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory

Molecular genetics & genomic medicine, 2019-03, Vol.7 (3), p.e545-n/a [Peer Reviewed Journal]

2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2019. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.545 ;PMID: 30706702

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10
Analyzing false‐negative results detected in low‐risk non‐invasive prenatal screening cases
Analyzing false‐negative results detected in low‐risk non‐invasive prenatal screening cases
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Analyzing false‐negative results detected in low‐risk non‐invasive prenatal screening cases

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1185-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals, Inc. ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2020. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1185 ;PMID: 32067421

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11
Relationship between early‐life nutrition and ages at menarche and first pregnancy, and childbirth rates of young adults: Evidence from APCAPS in India
Relationship between early‐life nutrition and ages at menarche and first pregnancy, and childbirth rates of young adults: Evidence from APCAPS in India
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Relationship between early‐life nutrition and ages at menarche and first pregnancy, and childbirth rates of young adults: Evidence from APCAPS in India

Maternal and child nutrition, 2020-01, Vol.16 (1), p.e12854-n/a [Peer Reviewed Journal]

2019 The Authors Published by John Wiley & Sons, Ltd ;2019 The Authors Maternal & Child Nutrition Published by John Wiley & Sons, Ltd. ;COPYRIGHT 2020 John Wiley & Sons, Inc. ;ISSN: 1740-8695 ;EISSN: 1740-8709 ;DOI: 10.1111/mcn.12854 ;PMID: 31141837

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12
Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technology
Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technology
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Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technology

Molecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1340-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC. ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1340 ;PMID: 32573981

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13
Confined placental mosaicism of trisomy 6 detected through genome‐wide NIPT was associated with placental abruption
Confined placental mosaicism of trisomy 6 detected through genome‐wide NIPT was associated with placental abruption
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Confined placental mosaicism of trisomy 6 detected through genome‐wide NIPT was associated with placental abruption

Clinical case reports, 2021-12, Vol.9 (12), p.e05155-n/a [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Ltd. ;2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. ;2021. 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: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.5155 ;PMID: 34917372

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14
Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center
Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center
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Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center

Molecular genetics & genomic medicine, 2021-07, Vol.9 (7), p.e1711-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/mgg3.1711 ;PMID: 34057320

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15
Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China
Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China
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Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China

Molecular genetics & genomic medicine, 2018-11, Vol.6 (6), p.1015-1020 [Peer Reviewed Journal]

2018 The Authors. published by Wiley Periodicals, Inc. ;2018 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2018. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.477 ;PMID: 30230267

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