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Molecular Genetics & Genomic Medicine
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/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/mgg3.1279 ;PMID: 32463164Full text available |
| 2 |
Material Type: Article
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Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studiesMolecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1654-n/a [Peer Reviewed Journal]2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/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/mgg3.1654 ;PMID: 33755350Full text available |
| 3 |
Material Type: Article
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Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidenceMolecular genetics & genomic medicine, 2020-07, Vol.8 (7), p.e1297-n/a [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;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. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1297 ;PMID: 32383339Full text available |
| 4 |
Material Type: Article
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Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirthMolecular genetics & genomic medicine, 2023-08, Vol.11 (8), p.e2187-n/a [Peer Reviewed Journal]2023 The Authors. published by Wiley Periodicals LLC. ;2023 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2023. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.2187 ;PMID: 37073418Full text available |
| 5 |
Material Type: Article
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Evaluation of the clinical effects of non-invasive prenatal screening for diseases associated with aneuploidy and copy number variationMolecular genetics & genomic medicine, 2023-09, Vol.11 (9), p.e2200-e2200 [Peer Reviewed Journal]2023 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;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. ;2023 The Authors. published by Wiley Periodicals LLC. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.2200 ;PMID: 37354111Full text available |
| 6 |
Material Type: Article
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Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, ChinaMolecular genetics & genomic medicine, 2020-10, Vol.8 (10), p.e1446-n/a [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals LLC. ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;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. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1446 ;PMID: 32767744Full text available |
| 7 |
Material Type: Article
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Prenatal cell‐free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratoryMolecular genetics & genomic medicine, 2019-03, Vol.7 (3), p.e545-n/a [Peer Reviewed Journal]2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2019. 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/mgg3.545 ;PMID: 30706702Full text available |
| 8 |
Material Type: Article
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Analyzing false‐negative results detected in low‐risk non‐invasive prenatal screening casesMolecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1185-n/a [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals, Inc. ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;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. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1185 ;PMID: 32067421Full text available |
| 9 |
Material Type: Article
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Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technologyMolecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1340-n/a [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals LLC. ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;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. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1340 ;PMID: 32573981Full text available |
| 10 |
Material Type: Article
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Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single centerMolecular genetics & genomic medicine, 2021-07, Vol.9 (7), p.e1711-n/a [Peer Reviewed Journal]2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/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/mgg3.1711 ;PMID: 34057320Full text available |
| 11 |
Material Type: Article
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Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in ChinaMolecular 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: 30230267Full text available |
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