Results 1 - 20 of 334 for All Library Resources
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Material Type: Article
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Complete Hydatidiform Coexistent Term Twin PregnancyJournal of perinatology, 2001-02, Vol.21 (1), p.72-75 [Peer Reviewed Journal]Copyright Nature Publishing Group Feb 2001 ;Nature America, Inc. 2000. ;ISSN: 0743-8346 ;EISSN: 1476-5543 ;DOI: 10.1038/sj.jp.7200491Full text available |
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Non‐invasive prenatal screening for chromosomal abnormalities using circulating cell-free fetal DNA in maternal plasma: Current applications, limitations and prospectsThe Egyptian journal of medical human genetics, 2017-01, Vol.18 (1), p.1-7 [Peer Reviewed Journal]2016 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2016.07.004Full text available |
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Association between different morphological types and abnormal karyotypes in early pregnancy lossUltrasound in obstetrics & gynecology, 2011-02, Vol.37 (2), p.219 [Peer Reviewed Journal]Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.7681 ;PMID: 20503243Digital Resources/Online E-Resources |
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Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosisHuman genetics, 2012-03, Vol.131 (3), p.513-523 [Peer Reviewed Journal]The Author(s) 2011 ;COPYRIGHT 2012 Springer ;Springer-Verlag 2012 ;The Author(s) 2011. This article is published with open access at Springerlink.com. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any non commercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. info:eu-repo/semantics/openAccess ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-011-1095-5 ;PMID: 21975797Full text available |
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The effects of age and abnormal sperm count on the nondisjunction of spermatozoaJournal of assisted reproduction and genetics, 2000, Vol.17 (1), p.51-59 [Peer Reviewed Journal]2000 INIST-CNRS ;Copyright Kluwer Academic Publishers Jan 2000 ;Plenum Publishing Corporation 2000 ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1023/A:1009454114973 ;PMID: 10754784 ;CODEN: JARGE4Full text available |
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Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriagesThe 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: 29255569Full text available |
| 7 |
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Increased nuchal translucency and pregnancy outcome: a retrospective study of 1063 consecutive singleton pregnancies in a single referral institutionPrenatal diagnosis, 2013-09, Vol.33 (9), p.856-862 [Peer Reviewed Journal]2013 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4143 ;PMID: 23613307Full text available |
| 8 |
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Non-invasive cell-free DNA-based approach for the diagnosis of clinical miscarriage: A retrospective studyBJOG : an international journal of obstetrics and gynaecology, 2024-01, Vol.131 (2), p.213 [Peer Reviewed Journal]2023 John Wiley & Sons Ltd. ;EISSN: 1471-0528 ;DOI: 10.1111/1471-0528.17629 ;PMID: 37533357Digital Resources/Online E-Resources |
| 9 |
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Parental origin and mechanisms of formation of triploidy: a study of 25 casesEuropean journal of human genetics : EJHG, 2000-12, Vol.8 (12), p.911-917 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2000 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5200572 ;PMID: 11175278Full text available |
| 10 |
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Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementEuropean journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1286-1293 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2015 ;Copyright © 2015 Macmillan Publishers Limited 2015 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2014.282 ;PMID: 25585704Full text available |
| 11 |
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Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variantsPrenatal diagnosis, 2023-02, Vol.43 (2), p.192 [Peer Reviewed Journal]2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6320 ;PMID: 36726284Digital Resources/Online E-Resources |
| 12 |
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Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcomePrenatal diagnosis, 2023-02, Vol.43 (2), p.183 [Peer Reviewed Journal]2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6302 ;PMID: 36600414Digital Resources/Online E-Resources |
| 13 |
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Chances and Challenges of New Genetic Screening Technologies (NIPT) in Prenatal Medicine from a Clinical Perspective: A Narrative ReviewGenes, 2021-03, Vol.12 (4), p.501 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12040501 ;PMID: 33805390Full text available |
| 14 |
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Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyPrenatal diagnosis, 2024-03, Vol.44 (3), p.304 [Peer Reviewed Journal]2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6529 ;PMID: 38411249Digital Resources/Online E-Resources |
| 15 |
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The Contribution of QF-PCR and Pathology Studies in the Diagnosis of Diandric Triploidy/Partial MoleDiagnostics (Basel), 2021-09, Vol.11 (10), p.1811 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2075-4418 ;EISSN: 2075-4418 ;DOI: 10.3390/diagnostics11101811 ;PMID: 34679509Full text available |
| 16 |
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Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challengeClinical epigenetics, 2017-10, Vol.9 (1), p.111-111, Article 111 [Peer Reviewed Journal]COPYRIGHT 2017 BioMed Central Ltd. ;Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 1868-7075 ;ISSN: 1868-7083 ;EISSN: 1868-7083 ;DOI: 10.1186/s13148-017-0410-y ;PMID: 29046733Full text available |
| 17 |
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Performance of first trimester screening for Trisomy 21 in twin pregnanciesPrenatal diagnosis, 2021-01, Vol.41 (2), p.210 [Peer Reviewed Journal]2020 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5857 ;PMID: 33128403Digital Resources/Online E-Resources |
| 18 |
Material Type: Article
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Frontiers in Medicine: Sequencing of Circulating Cell-free DNA during PregnancyThe New England journal of medicine, 2018-08, Vol.379 (5), p.464 [Peer Reviewed Journal]Copyright © 2018 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMra1705345Full text available |
| 19 |
Material Type: Article
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Higher limb asymmetry in deceased human fetuses and infants with aneuploidyScientific reports, 2014-01, Vol.4 (1), p.3703-3703, Article 3703 [Peer Reviewed Journal]Copyright Nature Publishing Group Jan 2014 ;Copyright © 2014, Macmillan Publishers Limited. All rights reserved 2014 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep03703 ;PMID: 24424506Full text available |
| 20 |
Material Type: Article
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Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancyEuropean journal of human genetics : EJHG, 2011-02, Vol.19 (2), p.231-234 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright Nature Publishing Group Feb 2011 ;Copyright © 2011 Macmillan Publishers Limited 2011 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2010.148 ;PMID: 20736977Full text available |
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