Cell-Free DNA Results Indicating Mosaic Monosomy X of Likely Maternal Origin: Impact on Genetic Counseling Practices and Patient Experiences.

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Title: Cell-Free DNA Results Indicating Mosaic Monosomy X of Likely Maternal Origin: Impact on Genetic Counseling Practices and Patient Experiences.
Authors: McBride A; Department of Clinical and Diagnostic Sciences, University of Alabama at Birmingham, Birmingham, Alabama, USA., Cannon A; Department of Clinical and Diagnostic Sciences, University of Alabama at Birmingham, Birmingham, Alabama, USA.; InformedDNA, St. Petersburg, Florida, USA., Prakash S; Division of Cardiology, Department of Internal Medicine, University of Texas Health Sciences Center at Houston, Houston, Texas, USA., Roberts AW; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, McGovern Medical School at UTHealth Houston, Houston, Texas, USA., Seasely A; Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, Alabama, USA., Hurst ACE; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA., Hendon L; Departments of Pediatrics and Obstetrics and Gynecology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Source: Prenatal diagnosis [Prenat Diagn] 2025 Apr; Vol. 45 (4), pp. 482-490. Date of Electronic Publication: 2025 Feb 15.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Cell-Free DNA Results Indicating Mosaic Monosomy X of Likely Maternal Origin: Impact on Genetic Counseling Practices and Patient Experiences.
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  Data: <searchLink fieldCode="AU" term="%22McBride+A%22">McBride A</searchLink>; Department of Clinical and Diagnostic Sciences, University of Alabama at Birmingham, Birmingham, Alabama, USA.<br /><searchLink fieldCode="AU" term="%22Cannon+A%22">Cannon A</searchLink>; Department of Clinical and Diagnostic Sciences, University of Alabama at Birmingham, Birmingham, Alabama, USA.; InformedDNA, St. Petersburg, Florida, USA.<br /><searchLink fieldCode="AU" term="%22Prakash+S%22">Prakash S</searchLink>; Division of Cardiology, Department of Internal Medicine, University of Texas Health Sciences Center at Houston, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Roberts+AW%22">Roberts AW</searchLink>; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, McGovern Medical School at UTHealth Houston, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Seasely+A%22">Seasely A</searchLink>; Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, Alabama, USA.<br /><searchLink fieldCode="AU" term="%22Hurst+ACE%22">Hurst ACE</searchLink>; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.<br /><searchLink fieldCode="AU" term="%22Hendon+L%22">Hendon L</searchLink>; Departments of Pediatrics and Obstetrics and Gynecology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
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  Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2025 Apr; Vol. 45 (4), pp. 482-490. <i>Date of Electronic Publication: </i>2025 Feb 15.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>8106540 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1097-0223 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2201973851%22">01973851 </searchLink><i>NLM ISO Abbreviation: </i>Prenat Diagn <i>Subsets: </i>MEDLINE
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        Value: 10.1002/pd.6760
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              Text: 2025 Apr
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