Search Results - Mathorne, Stine W.

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    Novel phenotype of syndromic premature ovarian insufficiency associated with TP63 molecular defect

    Novel phenotype of syndromic premature ovarian insufficiency associated with TP63 molecular defect by Mathorne, Stine W., Ravn, Pernille, Hansen, Dorte, Beck‐Nielsen, Signe S., Gjørup, Hans, Sørensen, Kristina P., Fagerberg, Christina R.

    Published in Clinical genetics
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