Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia by Massink, Maarten P.G., Créton, Marijn A., Spanevello, Francesca, Fennis, Willem M.M., Cune, Marco S., Savelberg, Sanne M.C., Nijman, Isaäc J., Maurice, Madelon M., van den Boogaard, Marie-José H., van Haaften, Gijs

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Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation by Ross, Jamila N., Ruigrok, Lisanne C., Fennis, Willem M.M., Cune, Marco S., Rosenberg, Antoine J.W.P., van Nunen, Annick B., Créton, Marijn A., Ploos van Amstel, Hans‐Kristian, van den Boogaard, Marie‐José J.H.

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Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome) by Monroe, Glen R, Kappen, Isabelle Fpm, Stokman, Marijn F, Terhal, Paulien A, van den Boogaard, Marie-José H, Savelberg, Sanne Mc, van der Veken, Lars T, van Es, Robert Jj, Lens, Susanne M, Hengeveld, Rutger C, Creton, Marijn A, Janssen, Nard G, Mink van der Molen, Aebele B, Ebbeling, Michelle B, Giles, Rachel H, Knoers, Nine V, van Haaften, Gijs

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Biallelic variants in POLR3GL cause endosteal hyperostosis and oligodontia by Terhal, Paulien A, Vlaar, Judith M, Middelkamp, Sjors, Nievelstein, Rutger A J, Nikkels, Peter G J, Ross, Jamila, Créton, Marijn, Bos, Jeroen W, Voskuil-Kerkhof, Elsbeth S M, Cuppen, Edwin, Knoers, Nine, van Gassen, Koen L I

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Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10 by Créton, Marijn, Wagener, Frank, Massink, Maarten, Fennis, Willem, Bloemen, Marjon, Schols, Jan, Aarts, Miranda, Molen, Aebele Mink, Haaften, Gijs, Boogaard, Marie José

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Oral Health-Related Quality of Life in Dutch Children Diagnosed with Oligodontia. A Cross-Sectional Study by Filius, Marieke A P, Cune, Marco S, Créton, Marijn, Vissink, Arjan, Raghoebar, Gerry M, Visser, Anita

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The association between WNT10A variants and dental development in patients with isolated oligodontia by Dhamo, Brunilda, Fennis, Willem, Créton, Marijn, Vucic, Strahinja, Cune, Marco, Ploos van Amstel, Hans Kristian, Wolvius, Eppo B, van den Boogaard, Marie-José, Ongkosuwito, Edwin M

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Concurrent manifestation of oligodontia and thrombocytopenia caused by a contiguous gene deletion in 12p13.2: A three‐generation clinical report by Ross, Jamila, Fennis, Willem, Leeuw, Nicole, Cune, Marco, Willemze, Annemieke, Rosenberg, Antoine, Ploos van Amstel, Hans‐Kristian, Créton, Marijn, Boogaard, Marie‐José

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Radiographic Features of Mandibular Trabecular Bone Structure in Hypodontia by Créton, Marijn, Geraets, Wil, Verhoeven, Jan Willem, van der Stelt, Paul F., Verhey, Hans, Cune, Marco

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Three-dimensional analysis of tooth dimensions in the MSX1-missense mutation by Créton, Marijn, van den Boogaard, Marie-José, Maal, Thomas, Verhamme, Luc, Fennis, Willem, Carels, Carine, Kuijpers-Jagtman, Anne Marie, Cune, Marco

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Dentofacial characteristics of patients with hypodontia by Créton, Marijn, Cune, Marco S., de Putter, Cornelis, Ruijter, Jan M., Kuijpers-Jagtman, Anne Marie

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