Search Results - "van Henten, Tessa M.A."

Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family by Elhaji, Youssef, van Henten, Tessa M.A., Ruivenkamp, Claudia A.L., Nightingale, Mathew, Santen, Gijs WE, Vos, Lydia E., Hull, Peter R.

“…Basan syndrome is an autosomal dominant genodermatosis characterized by congenital adermatoglyphia, transient congenital facial milia, neonatal acral bullae,…”
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Complication rate of wide local excision in patients with pT1a melanoma by Henten, Tessa M. A., Goris, Sandrine G., Kukutsch, Nicole A., Straver, Marieke E., Vos, Lydia E.

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