Prenatal diagnosis of trisomy 9 mosaicism possibly limited to fetal membranes
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference12 articles.
1. Trisomy 9 mosaicism in a newborn infant with multiple malformations
2. Autosomal mosaicism in amniotic fluid cells from a twin pregnancy
3. Mosaicism in amniotic fluid cell cultures: Classification and significance
4. (1982). Chromosome mosaicism and pseudomosaicism in prenatal cytogenetic diagnosis. In: , , (Eds). Clinical Genetics: Problems in Diagnosis and Counseling, New York: Academic Press, 77–106.
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1. Trisomy 9 mosaic syndrome: Sixteen additional patients with new and/or less commonly reported features, literature review, and suggested clinical guidelines;American Journal of Medical Genetics Part A;2021-05-10
2. Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis;Molecular Cytogenetics;2015-06-26
3. Current knowledge of prenatal diagnosis of mosaic autosomal trisomy in amniocytes: karyotype/phenotype correlations;Prenatal Diagnosis;2015-06-23
4. Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses;Taiwanese Journal of Obstetrics and Gynecology;2010-09
5. Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus;Clinical Genetics;2008-06-28
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