A Rare De Novo Robertsonian Translocation t(21q; 21q) in an Iranian Child With Down Syndrome: A Case Report
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DOI: 10.18502/acta.v57i8.2430
Abstract: Down syndrome or trisomy 21 is the most common genetic disorder with a prevalence of 1 in 700 live-born infants. It is characterized by the intellectual disability of varying range, developmental delay, distinctive facial features… read more here.
Keywords: 21q 21q; translocation 21q; child; case ... See more keywords