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1
Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study
Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study
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Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study

Prenatal diagnosis, 2017-06, Vol.37 (6), p.583 [Peer Reviewed Journal]

2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5051 ;PMID: 28406537

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2
Rapid diagnosis of aneuploidy using segmental duplication quantitative fluorescent PCR
Rapid diagnosis of aneuploidy using segmental duplication quantitative fluorescent PCR
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Rapid diagnosis of aneuploidy using segmental duplication quantitative fluorescent PCR

PloS one, 2014-03, Vol.9 (3), p.e88932-e88932 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Kong 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. ;2014 Kong et al 2014 Kong et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0088932 ;PMID: 24625828

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3
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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4
Genetic syndromes associated with isolated fetal growth restriction
Genetic syndromes associated with isolated fetal growth restriction
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Genetic syndromes associated with isolated fetal growth restriction

Prenatal diagnosis, 2020-03, Vol.40 (4), p.432 [Peer Reviewed Journal]

2019 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5635 ;PMID: 31891188

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5
Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases
Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases
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Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases

Journal of assisted reproduction and genetics, 2018-02, Vol.35 (2), p.265-271 [Peer Reviewed Journal]

Springer Science+Business Media, LLC 2017 ;Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2017). All Rights Reserved. ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-017-1069-1 ;PMID: 29086320

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6
Accuracy of first-trimester combined test in screening for trisomies 21, 18 and 13
Accuracy of first-trimester combined test in screening for trisomies 21, 18 and 13
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Accuracy of first-trimester combined test in screening for trisomies 21, 18 and 13

Ultrasound in obstetrics & gynecology, 2017-06, Vol.49 (6), p.714 [Peer Reviewed Journal]

Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.17283 ;PMID: 27549925

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7
Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review
Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review
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Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review

Prenatal diagnosis, 2017-11, Vol.37 (11), p.1061 [Peer Reviewed Journal]

2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5160 ;PMID: 28944967

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8
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
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Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.521-526 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group May 2012 ;Copyright © 2012 Macmillan Publishers Limited 2012 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2011.246 ;PMID: 22234154

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9
Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations
Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations
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Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations

Journal of human genetics, 2015-03, Vol.60 (3), p.133-137 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2015 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2014.116 ;PMID: 25566756

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10
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
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Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age

Journal of clinical laboratory analysis, 2020-04, Vol.34 (4), p.e23117-n/a [Peer Reviewed Journal]

2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals, Inc. ;2020. 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: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.23117 ;PMID: 31762079

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11
The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use
The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use
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The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use

PloS one, 2017-06, Vol.12 (6), p.e0178113-e0178113 [Peer Reviewed Journal]

COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 D’ippolito 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 D’ippolito et al 2017 D’ippolito et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0178113 ;PMID: 28604823

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12
Genetic analysis of products of conception using a HLPA/SNP-array strategy
Genetic analysis of products of conception using a HLPA/SNP-array strategy
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Genetic analysis of products of conception using a HLPA/SNP-array strategy

Molecular cytogenetics, 2019-09, Vol.12 (1), p.40-40, Article 40 [Peer Reviewed Journal]

The Author(s). 2019. ;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/s13039-019-0452-2 ;PMID: 31687045

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13
Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses
Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses
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Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses

Biopolimery i kletka, 2015, Vol.31 (1), p.38-45 [Peer Reviewed Journal]

2015. 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: 0233-7657 ;EISSN: 1993-6842 ;DOI: 10.7124/bc.0008CB

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14
The impact of Down syndrome screening on Taiwanese Down syndrome births: a nationwide retrospective study and a screening result from a single medical centre
The impact of Down syndrome screening on Taiwanese Down syndrome births: a nationwide retrospective study and a screening result from a single medical centre
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The impact of Down syndrome screening on Taiwanese Down syndrome births: a nationwide retrospective study and a screening result from a single medical centre

PloS one, 2013-09, Vol.8 (9), p.e75428-e75428 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Lin et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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. ;2013 Lin et al 2013 Lin et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0075428 ;PMID: 24147155

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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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16
Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages
Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages
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Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages

The Pan African medical journal, 2017, Vol.28 (99), p.99-99 [Peer Reviewed Journal]

Wiem Ayed et al. 2017. This work is licensed under the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/3.0/ ) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Distributed under a Creative Commons Attribution 4.0 International License ;Wiem Ayed et al. 2017 ;ISSN: 1937-8688 ;EISSN: 1937-8688 ;DOI: 10.11604/pamj.2017.28.99.11879 ;PMID: 29255569

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17
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
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15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies

Case reports in pediatrics, 2018-01, Vol.2018, p.8702568-5 [Peer Reviewed Journal]

Copyright © 2018 Hui-Fang Zhou et al. ;Copyright © 2018 Hui-Fang Zhou et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2018 Hui-Fang Zhou et al. 2018 ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2018/8702568 ;PMID: 30538881

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