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Results 1 - 20 of 6,692  for All Library Resources

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1
Normal umbilical artery doppler values in 18-22 week old fetuses with single umbilical artery
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Normal umbilical artery doppler values in 18-22 week old fetuses with single umbilical artery

Scientific reports, 2023-06, Vol.13 (1), p.10477-10477, Article 10477 [Peer Reviewed Journal]

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. ;The Author(s) 2023 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-023-37691-z ;PMID: 37380720

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2
Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges
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Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges

Genetics in medicine, 2017-11, Vol.19 (11), p.1207-1216 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2017 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.33 ;PMID: 28518170

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3
Exome sequencing for structurally normal fetuses-yields and ethical issues
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Exome sequencing for structurally normal fetuses-yields and ethical issues

European journal of human genetics : EJHG, 2023-02, Vol.31 (2), p.164-168 [Peer Reviewed Journal]

2022. The Author(s), under exclusive licence to European Society of Human Genetics. ;The Author(s), under exclusive licence to European Society of Human Genetics 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;The Author(s), under exclusive licence to European Society of Human Genetics 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-022-01169-9 ;PMID: 36071243

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4
A peptide-based viral inactivator inhibits Zika virus infection in pregnant mice and fetuses
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A peptide-based viral inactivator inhibits Zika virus infection in pregnant mice and fetuses

Nature communications, 2017-07, Vol.8 (1), p.15672-15672, Article 15672 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2017 ;Copyright © 2017, The Author(s) 2017 The Author(s) ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms15672 ;PMID: 28742068

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5
The prevalence of genetic diagnoses in fetuses with severe congenital heart defects
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The prevalence of genetic diagnoses in fetuses with severe congenital heart defects

Genetics in medicine, 2020-07, Vol.22 (7), p.1206-1214 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-0791-8 ;PMID: 32341573

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6
In vivo assessment of placental and brain volumes in growth-restricted fetuses with and without fetal Doppler changes using quantitative 3D MRI
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In vivo assessment of placental and brain volumes in growth-restricted fetuses with and without fetal Doppler changes using quantitative 3D MRI

Journal of perinatology, 2017-12, Vol.37 (12), p.1278-1284 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2017 ;Nature America, Inc., part of Springer Nature. 2017. ;ISSN: 0743-8346 ;EISSN: 1476-5543 ;DOI: 10.1038/jp.2017.129 ;PMID: 28837138

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7
Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype-phenotype correlations
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Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype-phenotype correlations

European journal of human genetics : EJHG, 2022-04, Vol.30 (4), p.428-438 [Peer Reviewed Journal]

2021. The Author(s). ;The Author(s) 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. ;The Author(s) 2021 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-021-01012-7 ;PMID: 34974531

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8
Ready or not, genomic screening of fetuses is already here
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Ready or not, genomic screening of fetuses is already here

Genetics in medicine, 2024-01, Vol.26 (1), p.101008-101008, Article 101008 [Peer Reviewed Journal]

ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1016/j.gim.2023.101008 ;PMID: 37860970

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9
Neural tube defects and uterus development in human fetuses
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Neural tube defects and uterus development in human fetuses

Scientific reports, 2022-08, Vol.12 (1), p.14051-14051, Article 14051 [Peer Reviewed Journal]

The Author(s) 2022. 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. ;The Author(s) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-18431-1 ;PMID: 35982132

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10
Predicting birth weight in fetuses with gastroschisis
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Predicting birth weight in fetuses with gastroschisis

Journal of perinatology, 2018-02, Vol.38 (2), p.122-126 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2018 ;ISSN: 0743-8346 ;EISSN: 1476-5543 ;DOI: 10.1038/jp.2017.171 ;PMID: 29266095

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11
Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
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Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses

Scientific reports, 2024-05, Vol.14 (1), p.10854-10854 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-60684-5 ;PMID: 38740788

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12
Prognosis factors for survival in fetuses with prenatally diagnosed megacystis
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Prognosis factors for survival in fetuses with prenatally diagnosed megacystis

Journal of perinatology, 2022-05, Vol.42 (5), p.667-668 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Nature America, Inc. 2021. ;ISSN: 0743-8346 ;EISSN: 1476-5543 ;DOI: 10.1038/s41372-021-01201-8 ;PMID: 34482381

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13
Detection of CWD prions in naturally infected white-tailed deer fetuses and gestational tissues by PMCA
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Detection of CWD prions in naturally infected white-tailed deer fetuses and gestational tissues by PMCA

Scientific reports, 2021-09, Vol.11 (1), p.18385-18385, Article 18385 [Peer Reviewed Journal]

2021. The Author(s). ;The Author(s) 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. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-97737-y ;PMID: 34526562

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14
Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation
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Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

Genetics in medicine, 2020-11, Vol.22 (11), p.1887-1891 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2020. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-0872-8 ;PMID: 32565546

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15
H19 lncRNA alters methylation and expression of Hnf4α in the liver of metformin-exposed fetuses
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H19 lncRNA alters methylation and expression of Hnf4α in the liver of metformin-exposed fetuses

Cell death & disease, 2017-12, Vol.8 (12), p.e3175-e3175 [Peer Reviewed Journal]

Copyright © 2017 The Author(s) 2017 The Author(s) ;ISSN: 2041-4889 ;EISSN: 2041-4889 ;DOI: 10.1038/cddis.2017.392 ;PMID: 29215608

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16
Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs
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Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs

European journal of human genetics : EJHG, 2016-05, Vol.24 (5), p.645-651 [Peer Reviewed Journal]

Copyright Nature Publishing Group May 2016 ;Copyright © 2016 Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2015.193 ;PMID: 26328504

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17
Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies
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Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies

Genetics in medicine, 2019-05, Vol.21 (5), p.1065-1073 [Peer Reviewed Journal]

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. ;The Author(s) 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0298-8 ;PMID: 30293990

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18
Early pregnancy maternal progesterone administration alters pituitary and testis function and steroid profile in male fetuses
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Article
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Early pregnancy maternal progesterone administration alters pituitary and testis function and steroid profile in male fetuses

Scientific reports, 2020-12, Vol.10 (1), p.21920-12, Article 21920 [Peer Reviewed Journal]

The Author(s) 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. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-78976-x ;PMID: 33318609

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19
Segmental aneuploidies in fetuses with isolated echogenic intracardiac focus among women younger than 35 years
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Segmental aneuploidies in fetuses with isolated echogenic intracardiac focus among women younger than 35 years

Scientific reports, 2020-06, Vol.10 (1), p.10496-10496, Article 10496 [Peer Reviewed Journal]

The Author(s) 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. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-67501-9 ;PMID: 32591622

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20
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings
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Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings

European journal of human genetics : EJHG, 2013-09, Vol.21 (9), p.936-942 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2013 ;Copyright © 2013 Macmillan Publishers Limited 2013 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2012.285 ;PMID: 23321623

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