Genetic Risk Factors for Atypical Femoral Fractures (AFFs): A Systematic Review by Nguyen, Hanh H, van de Laarschot, Denise M, Verkerk, Annemieke JMH, Milat, Frances, Zillikens, M Carola, Ebeling, Peter R

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Functional annotation of the human retinal pigment epithelium transcriptome by Booij, Judith C, van Soest, Simone, Swagemakers, Sigrid M A, Essing, Anke H W, Verkerk, Annemieke J M H, van der Spek, Peter J, Gorgels, Theo G M F, Bergen, Arthur A B

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Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients by Zhou, Wei, Rooij, Jeroen GJ, Laarschot, Denise M, Zervou, Zografia, Bruggenwirth, Hennie, Appelman‐Dijkstra, Natasha M, Ebeling, Peter R, Demirdas, Serwet, Verkerk, Annemieke JMH, Zillikens, M Carola

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An Activating Mutation in the Kinase Homology Domain of the Natriuretic Peptide Receptor-2 Causes Extremely Tall Stature Without Skeletal Deformities by Hannema, Sabine E, van Duyvenvoorde, Hermine A, Premsler, Thomas, Yang, Ruey-Bing, Mueller, Thomas D, Gassner, Birgit, Oberwinkler, Heike, Roelfsema, Ferdinand, Santen, Gijs W. E, Prickett, Timothy, Kant, Sarina G, Verkerk, Annemieke J. M. H, Uitterlinden, André G, Espiner, Eric, Ruivenkamp, Claudia A. L, Oostdijk, Wilma, Pereira, Alberto M, Losekoot, Monique, Kuhn, Michaela, Wit, Jan M

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Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy by Verkerk, Annemieke J.M.H., Schot, Rachel, Dumee, Belinda, Schellekens, Karlijn, Swagemakers, Sigrid, Bertoli-Avella, Aida M., Lequin, Maarten H., Dudink, Jeroen, Govaert, Paul, van Zwol, A.L., Hirst, Jennifer, Wessels, Marja W., Catsman-Berrevoets, Coriene, Verheijen, Frans W., de Graaff, Esther, de Coo, Irenaeus F.M., Kros, Johan M., Willemsen, Rob, Willems, Patrick J., van der Spek, Peter J., Mancini, Grazia M.S.

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Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report by de Vree, Paula Jp, Simon, Marleen Eh, van Dooren, Marieke F, Stoevelaar, Gerda Ht, Hilkmann, José Tw, Rongen, Michel A, Huijbregts, Gido Cm, Verkerk, Annemieke Jmh, Poddighe, Pino J

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Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family by Mescheriakova, Julia Y, Verkerk, Annemieke JMH, Amin, Najaf, Uitterlinden, André G, van Duijn, Cornelia M, Hintzen, Rogier Q

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Boston type craniosynostosis: Report of a second mutation in MSX2 by Florisson, Joyce M.G., Verkerk, Annemieke J.M.H., Huigh, Daphne, Hoogeboom, A. Jeannette M., Swagemakers, Sigrid, Kremer, Andreas, Heijsman, Daphne, Lequin, Maarten H., Mathijssen, Irene M.J., van der Spek, Peter J.

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A novel mutation in FGFR2 by Goos, Jacqueline A. C., van den Ouweland, Ans M. W., Swagemakers, Sigrid M. A., Verkerk, Annemieke J. M. H., Hoogeboom, A. Jeannette M., van Veelen, Marie-Lise C., Mathijssen, Irene M. J., van der Spek, Peter J.

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Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome by Florisson, Joyce M.G., Mathijssen, Irene M.J., Dumee, Belinda, Hoogeboom, Jeannette A.M., Poddighe, Pino J., Oostra, Ben A., Frijns, Jean Pierre, Koster, Linda, de Klein, Annelies, Eussen, Bert, de Vries, Bert B.A., Swagemakers, Sigrid, van der Spek, Peter J., Verkerk, Annemieke J.M.H.

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A bone overgrowth disorder due to a gain-of-function mutation in the kinase homology domain of guanylyl cyclase B, the receptor for CNP by Kuhn, Michaela, Premsler, Thomas, Yang, Ruey-Bing, Mueller, Thomas D, Gaßner, Birgit, Oberwinkler, Heike, Hannema, Sabine E, van Duyvenvoorde, Hermine A, Roelfsema, Ferdinand, Santen, Gijs WE, Prickett, Timothy, Kant, Sarina G, Verkerk, Annemieke JMH, Uitterlinden, André G, Espiner, Eric, Ruivenkamp, Claudia AL, Oostdijk, Wilma, Pereira, Alberto M, Losekoot, Monique, Wit, Jan M

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