Noonan Syndrome: Comparing Mutation-Positive with Mutation-Negative Dutch Patients

Por Croonen, E.A., Nillesen, W., Schrander, C., Jongmans, M., Scheffer, H., Noordam, C., Draaisma, J.M.T., van der Burgt, I., Yntema, H.G.
Publicado em 2013

Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.

Por Yntema, H G, Hamel, B C, Smits, A P, van Roosmalen, T, van den Helm, B, Kremer, H, Ropers, H H, Smeets, D F, van Bokhoven, H
Publicado em 1998

Occult Breast Cancer due to Multiple Calcified Hamartomas in a Patient with Cowden Syndrome

Por Gómez García, E. B., Lobbes, M. B. I., van de Vijver, K., Keymeulen, K., van der Ent, F., Yntema, H. G., Tjan-Heijnen, V. C., Boetes, C.
Publicado em 2012

Intra-individual stability over time of standardized anti-Müllerian hormone in FMR1 premutation carriers

Por Spath, M.A., Feuth, T.B., Allen, E.G., Smits, A.P.T., Yntema, H.G., van Kessel, A. Geurts, Braat, D.D.M., Sherman, S.L., Thomas, C.M.G.
Publicado em 2011

Chromosomal copy number changes in patients with non‐syndromic X linked mental retardation detected by array CGH

Por Lugtenberg, D, de Brouwer, A P M, Kleefstra, T, Oudakker, A R, Frints, S G M, Schrander‐Stumpel, C T R M, Fryns, J P, Jensen, L R, Chelly, J, Moraine, C, Turner, G, Veltman, J A, Hamel, B C J, de Vries, B B A, van Bokhoven, H, Yntema, H G
Publicado em 2006

Update on Kleefstra Syndrome

Por Willemsen, M.H., Vulto-van Silfhout, A.T., Nillesen, W.M., Wissink-Lindhout, W.M., van Bokhoven, H., Philip, N., Berry-Kravis, E.M., Kini, U., van Ravenswaaij-Arts, C.M.A., Delle Chiaie, B., Innes, A.M.M., Houge, G., Kosonen, T., Cremer, K., Fannemel, M., Stray-Pedersen, A., Reardon, W., Ignatius, J., Lachlan, K., Mircher, C., Helderman van den Enden, P.T.J.M., Mastebroek, M., Cohn-Hokke, P.E., Yntema, H.G., Drunat, S., Kleefstra, T.
Publicado em 2012