Hydatidiform mole and triploidy: the role of genomic imprinting in placental development
Author:
Publisher
Oxford University Press (OUP)
Subject
Obstetrics and Gynaecology,Reproductive Medicine
Link
http://academic.oup.com/humupd/article-pdf/11/2/137/2294237/dmh060.pdf
Reference41 articles.
1. Application of gene amplification by polymerase chain reaction to genetic analysis of molar mitochondrial DNA: The detection of anuclear empty ovum as the cause of complete mole
2. Recurrent triploidy of maternal origin
3. Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis
4. Three different origins for apparent triploid/diploid mosaics
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1. Dietary Factors and Incidence of Hydatidiform Mole: An Ecological Study;Nutrition and Cancer;2022-05-27
2. Abortion and Chromosomal Anomalies;Benirschke's Pathology of the Human Placenta;2021-12-08
3. The Contribution of QF-PCR and Pathology Studies in the Diagnosis of Diandric Triploidy/Partial Mole;Diagnostics;2021-09-30
4. Germline NLRP7 mutations: genomic imprinting and hydatidiform mole;Virchows Archiv;2020-06-23
5. Heterozygous/dispermic complete mole confers a significantly higher risk for post-molar gestational trophoblastic disease;Modern Pathology;2020-05-13
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