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47, XYY mosaic karyotype and congenital absence of bilateral vas deferens Case report

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NIAID Data Ecosystem2026-03-13 收录
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We report a rare case of infertility presenting with a 47, XYY mosaicism and congenital bilateral absence of vas deferens. With our patient's informed written consent, we performed a complete set of genetic tests for male infertility.

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2022-01-24
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