General obstetrics and gynecologyConfined placental mosaicism and intrauterine growth retardation: A case-control analysis of placentas at delivery☆
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Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study
2021, American Journal of Obstetrics and GynecologyCitation Excerpt :There are several pathologic mechanisms leading to FGR, and identifying these mechanisms is required for optimal management of the pregnancy. Notably, one cause can be the presence of chromosomal abnormalities associated with structural anomalies, which account for 7% to 30% of FGR cases.9–11 However, chromosomal anomalies can also be present when no structural anomalies associated with FGR are detected on ultrasound,9,12 and therefore, prenatal invasive genetic testing may be offered in cases of isolated FGR to exclude genetic disorders.
Development of the Placenta and Its Circulation
2019, Fetal Medicine: Basic Science and Clinical PracticeMosaicism between trophectoderm and inner cell mass
2017, Fertility and SterilityPlacental features in intrauterine growth retardation
2013, Journal de Gynecologie Obstetrique et Biologie de la ReproductionInvestigation of confined placental mosaicism by CGH in IVF and ICSI pregnancies
2012, PlacentaCitation Excerpt :In approximately 50% of cases, the extra X chromosome is of maternal origin [49]. In CPM, double trisomy has been reported and was associated with IUGR [50]. Mosaic trisomy 13 was reported in one IVF–ICSI placenta through CVS [20].
Genome-Wide Detection of Uniparental Disomy in a Fetus with Intrauterine Growth Restriction Using Genotyping Microarrays
2009, Taiwanese Journal of Obstetrics and Gynecology
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Supported in part by the William Randolph Hearst Fund at Harvard Medical School.