Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference51 articles.
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4. Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.
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1. Partial tetrasomy 18 mosaicism: Pre and postnatal diagnosis of a unique pattern;Taiwanese Journal of Obstetrics and Gynecology;2022-01
2. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2017-12
3. Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies;Gene;2015-03
4. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p;Taiwanese Journal of Obstetrics and Gynecology;2014-03
5. Prenatal diagnosis of mosaic tetrasomy 18p;Taiwanese Journal of Obstetrics and Gynecology;2012-12
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