Androgenetic complete mole with trisomy 13: Report of a case with microsatellite genotyping and review of the literature
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Pathology and Forensic Medicine
Reference15 articles.
1. Chromosomal anomalies in abnormal human pregnancies;Brajenović-Milić;Fetal Diagn. Ther.,1998
2. Trisomy 13 appearing as a mimic of a triploid partial mole;Curtin;J. Ultrasound Med.,2001
3. Complete hydatidiform mole retaining a chromosome 11 of maternal origin: molecular genetic analysis of a case;Fisher;Mod. Pathol.,2004
4. A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution;Helwani;Hum. Genet.,1999
5. P57KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions;Hoffner;Hum. Pathol.,2008
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1. Aneuploidy is frequent in heterozygous diploid and triploid hydatidiform moles;Scientific Reports;2024-03-22
2. Genetics of gestational trophoblastic disease;Best Practice & Research Clinical Obstetrics & Gynaecology;2021-07
3. Parental contribution to trisomy in heterozygous androgenetic complete moles;Scientific Reports;2020-10-13
4. A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin;Journal of Obstetrics and Gynaecology Research;2018-02-13
5. The genetics of gestational trophoblastic disease: a rare complication of pregnancy;Cancer Genetics;2012-03
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