Maternal uniparental heterodisomy for chromosome 2: detection through ?atypical? maternal AFP/hCG levels, with an update on a previous case
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference24 articles.
1. TRISOMY 2: CONFINED PLACENTAL MOSAICISM IN A FETUS WITH INTRAUTERINE GROWTH RETARDATION
2. Cytogenetic analysis of chorionic villi for prenatal diagnosis: An ACC collaborative study of U.K. data
3. Fetoplacental chromosomal discrepancy
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1. Maternal Uniparental Isodisomy of Chromosome 2 Leading to Homozygous Variants in SPR and ZNF142: A Case Report and Review of the UPD2 Literature;Global Medical Genetics;2024-01
2. Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with positive NIPT and CVS results for trisomy 2, maternal uniparental disomy 2, perinatal progressive decrease of the aneuploid cell line, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, intrauterine growth restriction and a favorable fetal outcome;Taiwanese Journal of Obstetrics and Gynecology;2023-07
3. Prenatal Detection of Trisomy 2: Considerations for Genetic Counseling and Testing;Genes;2023-04-14
4. Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler–Najjar syndrome type I and long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency;American Journal of Medical Genetics Part A;2022-02-24
5. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2021-04-20
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