Current knowledge of prenatal diagnosis of mosaic autosomal trisomy in amniocytes: karyotype/phenotype correlations
Author:
Affiliation:
1. Departments of Pediatrics; Santa Clara Valley Medical Center; San Jose CA USA
2. Obstetrics and Gynecology; Santa Clara Valley Medical Center; San Jose CA USA
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference142 articles.
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2. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations;Hsu;Prenat Diagn,1997
3. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20, and 21: karyotype-phenotype correlations;Wallerstein;Prenat Diagn,2000
4. European collaborative study on prenatal diagnosis: mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures;Bui;Prenat Diagn,1984
5. Prenatal diagnosis of trisomy 2 mosaicism confirmed in foreskin fibroblasts;Casey;Am J Hum Genet,1990
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