Prenatal diagnosis of mosaic trisomy 9
Author:
Funder
National Science Council
Mackay Memorial Hospital
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference7 articles.
1. Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9;Chen;Prenat Diagn,2003
2. Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature;Chen;Prenat Diagn,2004
3. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses;Chen;Taiwan J Obstet Gynecol,2010
4. Presenting physical characteristics, medical conditions, and developmental status of long-term survivors with trisomy 9 mosaicism;Bruns;Am J Med Genet,2011
5. Prenatal diagnosis of trisomy 9 mosaicism: two new cases;Merino;Prenat Diagn,1993
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1. Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2022-01
2. 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
3. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2021-04-20
4. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2015-11-23
5. Current knowledge of prenatal diagnosis of mosaic autosomal trisomy in amniocytes: karyotype/phenotype correlations;Prenatal Diagnosis;2015-06-23
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