Challenges in diagnosing hydatidiform moles: a review of promising molecular biomarkers
Author:
Affiliation:
1. Department of Gynaecology and Obstetrics, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou City, Zhejiang Province, China
Funder
the Key Research and Development Program of Zhejiang Province, China
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology,Molecular Medicine,Pathology and Forensic Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/14737159.2022.2118050
Reference128 articles.
1. Hydatidiform Moles: Genetic Basis and Precision Diagnosis
2. Complete moles have paternal chromosomes but maternal mitochondrial DNA
3. 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
4. Genetics of gestational trophoblastic disease
5. Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans
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1. Hematoxylin and Eosin Staining Helps Reduce Maternal Contamination in Short Tandem Repeat Genotyping for Hydatidiform Mole Diagnosis;International Journal of Gynecological Pathology;2023-08-11
2. Pathogenic role of Twist-1 protein in hydatidiform molar pregnancies and investigation of its potential diagnostic utility in complete moles;Diagnostic Pathology;2023-03-29
3. Gestação molar em paciente na perimenopausa – relato de caso;STUDIES IN HEALTH SCIENCES;2023-03-02
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