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- W2188894013 abstract "Results – Chromosomal analysis revealed free trisomy 21 karyotype in 95%, mosaic trisomy karyotype in 5%, and none with chromosome translocation. The parent of origin of chromosome 21 trisomy was determined in 85% of the cases. Nondisjunctional error was determined as maternal in 86% and paternal in 14% of the cases. Conclusion – Although the exact mechanism behind chromosome nondisjunction has not been very well described, but in the case of free chromosome 21 trisomy the exact reasons behind the nondisjunction may vary between female and male who passed this extra chromosome to their child. The knowledge of Down syndrome of parental origin is one of the basic steps to evaluate accurately the risk factors and etiology of meiotic nondisjunction." @default.
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- W2188894013 date "2004-01-01" @default.
- W2188894013 modified "2023-09-27" @default.
- W2188894013 title "PARENTAL ORIGIN OF MEIOTIC ERROR OF THE EXTRA CHROMOSOME 21 AS INDICATED BY SHORT TANDEM REPEAT (STR) POLYMORPHISMS IN DOWN SYNDROME" @default.
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