Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity von van Bever, Yolande, Wolffenbuttel, Katja P., Brüggenwirth, Hennie T., Blom, Eric, de Klein, Annelies, Eussen, Bert H.J., van der Windt, Florijn, Hannema, Sabine E., Dessens, Arianne B., Dorssers, Lambert C.J., Biermann, Katharina, Hersmus, Remko, de Rijke, Yolanda B., Looijenga, Leendert H.J.

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Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity von Knijnenburg, Jeroen, Uytdewilligen, Madiek E.W, van Hassel, Daniella A.C.M, Oostenbrink, Rianne, Eussen, Bert H.J, de Klein, Annelies, Brooks, Alice S, van Zutven, Laura J.C.M

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Quantification of MYCN, DDX1, and NAG Gene Copy Number in Neuroblastoma Using a Real-Time Quantitative PCR Assay von De Preter, Katleen, Speleman, Frank, Combaret, Valérie, Lunec, John, Laureys, Geneviève, Eussen, Bert H J, Francotte, Nadine, Board, Julian, Pearson, Andy D J, De Paepe, Anne, Van Roy, Nadine, Vandesompele, Jo

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Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder von Verkerk, Annemieke J.M.H., Mathews, Carol A., Joosse, Marijke, Eussen, Bert H.J., Heutink, Peter, Oostra, Ben A.

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Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere von Warburton, Peter E., Dolled, Marisa, Mahmood, Radma, Alonso, Alicia, Li, Shulan, Naritomi, Kenji, Tohma, Takaya, Nagai, Toshiro, Hasegawa, Tomonobu, Ohashi, Hirofumi, Govaerts, Lutgarde C.P., Eussen, Bert H.J., Van Hemel, Jan O., Lozzio, Carmen, Schwartz, Stuart, Dowhanick-Morrissette, Jennifer J., Spinner, Nancy B., Rivera, Horacio, Crolla, John A., Yu, Chih-yu, Warburton, Dorothy

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Characterization of a Zinc-Finger Protein and Its Association With Apoptosis in Prostate Cancer Cells von Chang, Glenn T. G., Steenbeek, Martine, Schippers, Esther, Blok, Leen J., van Weerden, Wytske M., van Alewijk, Dirk C. J. G., Eussen, Bert H. J., van Steenbrugge, Gert J., Brinkmann, Albert O.

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The murine CYLN2 gene : Genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region von HOOGENRAAD, C. C, EUSSEN, B. H. J, LANGEVELD, A, VAN HAPEREN, R, WINTERBERG, S, WOUTERS, C. H, GROSVELD, F, DE ZEEUW, C. I, GALJART, N

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Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspring von Galjaard, Robert‐Jan H., van der Linde, Herma C., Eussen, Bert H. J., de Vries, Bert B. A., Wouters, Cokkie H., Oostra, Ben A., Graaff, Esther de, Heutink, Peter

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Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data von Hamel, B C, Smits, A P, de Graaff, E, Smeets, D F, Schoute, F, Eussen, B H, Knight, S J, Davies, K E, Assman-Hulsmans, C F, Oostra, B A

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Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate‐cancer progression von Chang, Glenn T.G., Tapsi, Nita, Steenbeek, Martine, Blok, Leen J., van Weerden, Wytske M., van Alewijk, Dirk C.J.G., Eussen, Bert H.J., van Steenbrugge, Gert J., Brinkmann, Albert O.

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The MurineCYLN2Gene: Genomic Organization, Chromosome Localization, and Comparison to the Human Gene That Is Located within the 7q11.23 Williams Syndrome Critical Region von Hoogenraad, Casper C, Eussen, Bert H.J, Langeveld, An, van Haperen, Rien, Winterberg, Suzanne, Wouters, Cokkie H, Grosveld, Frank, De Zeeuw, Chris I, Galjart, Niels

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A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei von Van Opstal, Diane, Van Hemel, Jan O., Eussen, Bert H. J., Van Der Heide, Annet, Van Den Berg, Cardi, Veld, Peter A. In't, Los, Frans J.

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Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) von de Vries, Bert B.A., Eussen, Bert H.J., van Diggelen, Otto P., van der Heide, Annet, Deelen, Wouter H., Govaerts, Lutgarde C.P., Lindhout, Dick, Wouters, Cokkie H., Van Hemel, Jan O.

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An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito von Eussen, Bert H J, Bartalini, Gabriella, Bakker, Lida, Balestri, Paolo, Di Lucca, Carmela, Van Hemel, Jan O, Dauwerse, Hans, van den Ouweland, Ans M W, Ris-Stalpers, Carrie, Verhoef, Senno, Halley, Dicky J J, Fois, Alberto

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Limited size of the fragile X site shown by fluorescence in situ hybridization von Verkerk, Annemieke J. M. H., Eussen, Bert H. J., Van Hemel, Jan O., Oostra, Ben A.

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