Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features by Tucci, Valter, Kleefstra, Tjitske, Hardy, Andrea, Heise, Ines, Maggi, Silvia, Willemsen, Marjolein H, Hilton, Helen, Esapa, Chris, Simon, Michelle, Buenavista, Maria-Teresa, McGuffin, Liam J, Vizor, Lucie, Dodero, Luca, Tsaftaris, Sotirios, Romero, Rosario, Nillesen, Willy N, Vissers, Lisenka E L M, Kempers, Marlies J, Vulto-van Silfhout, Anneke T, Iqbal, Zafar, Orlando, Marta, Maccione, Alessandro, Lassi, Glenda, Farisello, Pasqualina, Contestabile, Andrea, Tinarelli, Federico, Nieus, Thierry, Raimondi, Andrea, Greco, Barbara, Cantatore, Daniela, Gasparini, Laura, Berdondini, Luca, Bifone, Angelo, Gozzi, Alessandro, Wells, Sara, Nolan, Patrick M

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X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers by Spath, Marian A., Nillesen, Willy N., Smits, Arie P.T., Feuth, Ton B., Braat, Didi D.M., van Kessel, Ad Geurts, Yntema, Helger G.

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Dominant [Beta]-catenin mutations cause intellectual disability with recognizable syndromic features by Tucci, Valter, Kleefstra, Tjitske, Hardy, Andrea, Heise, Ines, Maggi, Silvia, Willemsen, Marjolein H, Hilton, Helen, Esapa, Chris, Simon, Michelle, Buenavista, Maria-Teresa, McGuffin, Liam J, Vizor, Lucie, Dodero, Luca, Tsaftaris, Sotirios, Romero, Rosario, Nillesen, Willy N, Vissers, Lisenka E L M, Kempers, Marlies J, Vulto-van Silfhout, Anneke T, Iqbal, Zafar, Orlando, Marta, Maccione, Alessandro, Lassi, Glenda, Farisello, Pasqualina, Contestabile, Andrea, Tinarelli, Federico, Nieus, Thierry, Raimondi, Andrea, Greco, Barbara, Cantatore, Daniela, Gasparini, Laura, Berdondini, Luca, Bifone, Angelo, Gozzi, Alessandro, Wells, Sara, Nolan, Patrick M

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Diagnostic Genome Profiling in Mental Retardation by de Vries, Bert B.A., Pfundt, Rolph, Leisink, Martijn, Koolen, David A., Vissers, Lisenka E.L.M., Janssen, Irene M., Reijmersdal, Simon van, Nillesen, Willy M., Huys, Erik H.L.P.G., Leeuw, Nicole de, Smeets, Dominique, Sistermans, Erik A., Feuth, Ton, van Ravenswaaij-Arts, Conny M.A., van Kessel, Ad Geurts, Schoenmakers, Eric F.P.M., Brunner, Han G., Veltman, Joris A.

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Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndrome by Kleefstra, Tjitske, Koolen, David A., Nillesen, Willy M., de Leeuw, Nicole, Hamel, Ben C.J., Veltman, Joris A., Sistermans, Erik A., van Bokhoven, Hans, van Ravenswaay, Conny, de Vries, Bert B.A.

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