Global ETD Search
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Showing 1 to 1 of 1 for “"Síndrome de Swyer"”.
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Diferentes apresentações clínicas da Síndrome de Swyer: relatos de casos
x development caused by mutations in genes located in the Y chromosome. It’s typically described in female individuals with a 46XY karyotype and streak gonads, and it’s normally diagnosed in adolescence because of the absence of menstruation, with or without the spontaneous female sexual …