Prenatal diagnosis of a trisomy 7/maternal uniparental heterodisomy 7 mosaic fetus
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference10 articles.
1. 1998. Cytogenetics. Principles of medical genetics. 2nd edition. Baltimore: Williams and Wilkins. p 162-163.
2. Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
3. RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS
4. Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases
5. Maternal uniparental disomy 7 - review and further delineation of the phenotype
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1. Low-level mosaic trisomy 7 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 7 cell line and a favorable fetal outcome;Taiwanese Journal of Obstetrics and Gynecology;2024-07
2. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?;BMC Pregnancy and Childbirth;2024-05-03
3. Genetic counseling of non-invasive prenatal testing (NIPT) trisomy 7-positive pregnancies;Taiwanese Journal of Obstetrics and Gynecology;2024-05
4. Clinical manifestations and the prenatal diagnosis of trisomy 7 mosaicism: Two case reports;World Journal of Clinical Cases;2024-03-16
5. Performance of noninvasive prenatal testing for twin pregnancies in South China;Journal of Assisted Reproduction and Genetics;2023-07-22
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