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- W2358949399 abstract "SUMMARY A case of a triple X woman with two Down syndrome children is reported, where both sibs showed a karyotype with regular trisomy 21 by G banding. Karyotype of father is normal. Moreover, the karyo- type was realized in the triple X womens family to search for the presence of an aneuploidy. However, in all cases it was normal. Studies of the polimorphyc marker D21S11 were realized to find the meiotic and parental origin in both sibs. Results sugested a maternal non-disjunction in meiosis I. Posible me- chanisms of the recurrence of regular trisomy 21 in this family are discusse, and also the relationship of the trisomy 21 in both sibs with repect to the maternal trisomy X." @default.
- W2358949399 created "2016-06-24" @default.
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- W2358949399 date "2008-01-01" @default.
- W2358949399 modified "2023-09-26" @default.
- W2358949399 title "Reporte de un caso clínico Mujer Triple X con 2 hijos Down" @default.
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- W2358949399 hasPublicationYear "2008" @default.
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