Down Syndrome Resulting from a Rare non-Robertsonian Translocation t(11;21)(p13;q22)
Introduction: Down syndrome (DS) is a common genetic disorder, occurring in approximately 1 in 700 births. It results from an extra copy (triplication) of the whole or part of the long arm of chromosome 21 caused by different cytogenetic alterations: free trisomy, Robertsonian translocations, mosaic...
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Format: | Book |
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Faculdade de Medicina de São José do Rio Preto,
2021-08-01T00:00:00Z.
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A1234.567 |
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