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1
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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2
Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth
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Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth

BMC women's health, 2024-01, Vol.24 (1), p.42-12, Article 42 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1472-6874 ;EISSN: 1472-6874 ;DOI: 10.1186/s12905-023-02856-5 ;PMID: 38225596

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3
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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4
Triploidy and Routine Combined First Trimester Pregnancy Screening
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Triploidy and Routine Combined First Trimester Pregnancy Screening

Avicenna journal of medical biotechnology, 2019-01, Vol.11 (1), p.124-126 [Peer Reviewed Journal]

COPYRIGHT 2019 Avicenna Research Institute ;Copyright© 2019 Avicenna Research Institute 2019 ;ISSN: 2008-2835 ;EISSN: 2008-4625 ;PMID: 30800253

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5
Conceptualization, measurement, and effects of pregnancy-specific stress: review of research using the original and revised Prenatal Distress Questionnaire
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Conceptualization, measurement, and effects of pregnancy-specific stress: review of research using the original and revised Prenatal Distress Questionnaire

Journal of behavioral medicine, 2020-02, Vol.43 (1), p.16-33 [Peer Reviewed Journal]

Springer Science+Business Media, LLC, part of Springer Nature 2019 ;COPYRIGHT 2020 Springer ;Journal of Behavioral Medicine is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 0160-7715 ;EISSN: 1573-3521 ;DOI: 10.1007/s10865-019-00068-7 ;PMID: 31183596

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6
Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study
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Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study

BMC pregnancy and childbirth, 2024-01, Vol.24 (1), p.93-93, Article 93 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-024-06275-8 ;PMID: 38297236

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7
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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8
Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
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Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

BMC medical genomics, 2012-12, Vol.5 (1), p.57-57, Article 57 [Peer Reviewed Journal]

COPYRIGHT 2012 BioMed Central Ltd. ;COPYRIGHT 2012 BioMed Central Ltd. ;2012 Jiang 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 ©2012 Jiang et al.; licensee BioMed Central Ltd. 2012 Jiang et al.; licensee BioMed Central Ltd. ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/1755-8794-5-57 ;PMID: 23198897

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9
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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10
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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11
Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results
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Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results

BMC pregnancy and childbirth, 2022-11, Vol.22 (1), p.813-813, Article 813 [Peer Reviewed Journal]

The Author(s) 2022 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-022-05139-3 ;PMID: 36333674

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12
Antenatal depression and its potential causal mechanisms among pregnant mothers in Gondar town: application of structural equation model
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Antenatal depression and its potential causal mechanisms among pregnant mothers in Gondar town: application of structural equation model

BMC pregnancy and childbirth, 2020-03, Vol.20 (1), p.168-168, Article 168 [Peer Reviewed Journal]

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: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-020-02859-2 ;PMID: 32183726

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13
Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal age
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Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal age

Orphanet journal of rare diseases, 2024-02, Vol.19 (1), p.56-56 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-024-03066-4 ;PMID: 38336695

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14
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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15
Nonendocrine mechanisms of sex bias in rheumatic diseases
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Article
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Nonendocrine mechanisms of sex bias in rheumatic diseases

Nature reviews. Rheumatology, 2019-11, Vol.15 (11), p.673-686 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2019 ;ISSN: 1759-4790 ;EISSN: 1759-4804 ;DOI: 10.1038/s41584-019-0307-6 ;PMID: 31597952

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16
An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing
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An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing

PloS one, 2016-07, Vol.11 (7), p.e0159648-e0159648 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Wang 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 Wang et al 2016 Wang et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0159648 ;PMID: 27441628

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17
Evaluation of first trimester maternal serum inhibin-A for preeclampsia screening
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Evaluation of first trimester maternal serum inhibin-A for preeclampsia screening

PloS one, 2023-07, Vol.18 (7), p.e0288289-e0288289 [Peer Reviewed Journal]

Copyright: © 2023 Moungmaithong et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. ;COPYRIGHT 2023 Public Library of Science ;2023 Moungmaithong et al 2023 Moungmaithong et al ;2023 Moungmaithong 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. ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0288289 ;PMID: 37428792

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18
Maternal Bacteremia Caused by Staphylococcus Aureus With a Focus on Infective Endocarditis
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Maternal Bacteremia Caused by Staphylococcus Aureus With a Focus on Infective Endocarditis

Open forum infectious diseases, 2020-08, Vol.7 (8), p.ofaa239-ofaa239 [Peer Reviewed Journal]

The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. ;COPYRIGHT 2020 Oxford University Press ;The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2020 ;ISSN: 2328-8957 ;EISSN: 2328-8957 ;DOI: 10.1093/ofid/ofaa239 ;PMID: 32766382

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19
Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review
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Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review

BMC pregnancy and childbirth, 2019-10, Vol.19 (1), p.385-385, Article 385 [Peer Reviewed Journal]

The Author(s). 2019 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-019-2518-x ;PMID: 31660889

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20
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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