Results 1 - 20 of 43 for All Library Resources
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Material Type: Article
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A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidyPrenatal diagnosis, 2023-02, Vol.43 (2), p.133 [Peer Reviewed Journal]2023 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6298 ;PMID: 36588186Digital Resources/Online E-Resources |
| 2 |
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All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experiencePrenatal diagnosis, 2023-04, Vol.43 (4), p.527 [Peer Reviewed Journal]2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6314 ;PMID: 36647814Digital Resources/Online E-Resources |
| 3 |
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Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidiesPrenatal diagnosis, 2017-09, Vol.37 (9), p.916 [Peer Reviewed Journal]2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5112 ;PMID: 28688121Digital Resources/Online E-Resources |
| 4 |
Material Type: Article
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Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeksPrenatal diagnosis, 2011-01, Vol.31 (1), p.90-102 [Peer Reviewed Journal]Copyright © 2011 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;ISSN: 1097-0223 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2642 ;PMID: 21210483Full text available |
| 5 |
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Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twinsPrenatal diagnosis, 2018-04, Vol.38 (5), p.318 [Peer Reviewed Journal]2018 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5238 ;PMID: 29460287Digital Resources/Online E-Resources |
| 6 |
Material Type: Article
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Chromosomal mosaicism: Origins and clinical implications in preimplantation and prenatal diagnosisPrenatal diagnosis, 2021-04, Vol.41 (5), p.631 [Peer Reviewed Journal]2021 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5931 ;PMID: 33720449Digital Resources/Online E-Resources |
| 7 |
Material Type: Article
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Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluidPrenatal diagnosis, 2016-06, Vol.36 (6), p.576-583 [Peer Reviewed Journal]2016 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4830 ;PMID: 27084671Full text available |
| 8 |
Material Type: Article
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Cytogenetic analysis of 355 cases of fetal loss in different trimestersPrenatal diagnosis, 2011-02, Vol.31 (2), p.152-158 [Peer Reviewed Journal]Copyright © 2011 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;ISSN: 0197-3851 ;ISSN: 1097-0223 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2665 ;PMID: 21268033 ;CODEN: PRDIDMFull text available |
| 9 |
Material Type: Article
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Detection rates and residual risk for a postnatal diagnosis of an atypical chromosome aberration following combined first-trimester screeningPrenatal diagnosis, 2020-06, Vol.40 (7), p.852 [Peer Reviewed Journal]ISSN: 1097-0223 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5698Digital Resources/Online E-Resources |
| 10 |
Material Type: Article
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Discordant non-invasive prenatal testing (NIPT) - a systematic reviewPrenatal diagnosis, 2017-06, Vol.37 (6), p.527 [Peer Reviewed Journal]2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5049 ;PMID: 28382695Digital Resources/Online E-Resources |
| 11 |
Material Type: Article
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Evaluation of the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single centerPrenatal diagnosis, 2021-05, Vol.41 (6), p.690 [Peer Reviewed Journal]2021 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5908 ;PMID: 33480032Digital Resources/Online E-Resources |
| 12 |
Material Type: Article
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First-trimester sonographic findings in trisomy 18: a review of 53 casesPrenatal diagnosis, 2010-03, Vol.30 (3), p.256-259 [Peer Reviewed Journal]Copyright © 2010 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;Copyright (c) 2010 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;ISSN: 1097-0223 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2462 ;PMID: 20112232 ;CODEN: PRDIDMFull text available |
| 13 |
Material Type: Article
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Genetic syndromes associated with isolated fetal growth restrictionPrenatal 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: 31891188Digital Resources/Online E-Resources |
| 14 |
Material Type: Article
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High false-positive non-invasive prenatal screening results for sex chromosome abnormalities: Are maternal factors the culprit?Prenatal diagnosis, 2020-03, Vol.40 (4), p.463 [Peer Reviewed Journal]2019 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5529 ;PMID: 31318441Digital Resources/Online E-Resources |
| 15 |
Material Type: Article
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Identification of fetal aneuploidy with dual-probe fluorescence in situ hybridization analysis in circulating trophoblasts after enrichment using a high-sensitivity microfluidic platformPrenatal diagnosis, 2021-12, Vol.41 (13), p.1701 [Peer Reviewed Journal]2021 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6046 ;PMID: 34582049Digital Resources/Online E-Resources |
| 16 |
Material Type: Article
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Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidiesPrenatal diagnosis, 2017-10, Vol.37 (10), p.1017 [Peer Reviewed Journal]2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5138 ;PMID: 28801976Digital Resources/Online E-Resources |
| 17 |
Material Type: Article
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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 |
| 18 |
Material Type: Article
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International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosisPrenatal diagnosis, 2022-05, Vol.42 (6), p.796 [Peer Reviewed Journal]2022 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6157 ;PMID: 35583085Digital Resources/Online E-Resources |
| 19 |
Material Type: Article
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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 |
| 20 |
Material Type: Article
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Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective studyPrenatal 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: 28406537Digital Resources/Online E-Resources |
Results 1 - 20 of 43 for All Library Resources
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