The p63 gene in EEC and other syndromes

由 Brunner, H, Hamel, B, van Bokhoven, H
出版 2002

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

由 Barrow, L, van Bokhoven, H, Daack-Hirsch, S, Andersen, T, van Beersum, S E C, Gorlin, R, Murray, J
出版 2002

MicroRNA networks direct neuronal development and plasticity

由 Olde Loohuis, N. F. M., Kos, A., Martens, G. J. M., Van Bokhoven, H., Nadif Kasri, N., Aschrafi, A.
出版 2011

Long-term consequences of chronic fluoxetine exposure on the expression of myelination-related genes in the rat hippocampus

由 Kroeze, Y, Peeters, D, Boulle, F, van den Hove, D L A, van Bokhoven, H, Zhou, H, Homberg, J R
發表在 Transl Psychiatry (2016)

Long-term consequences of chronic fluoxetine exposure on the expression of myelination-related genes in the rat hippocampus

由 Kroeze, Y, Peeters, D, Boulle, F, van den Hove, D L A, van Bokhoven, H, Zhou, H, Homberg, J R
發表在 Transl Psychiatry (2015)

The small patella syndrome: description of five cases from three families and examination of possible allelism with familial patella aplasia-hypoplasia and nail-patella syndrome

由 BONGERS, E., VAN BOKHOVEN, H., VAN THIENEN, M.-N., KOOYMAN, M., VAN BEERSUM, S. E C, BOETES, C., KNOERS, N., HAMEL, B.
出版 2001

ΔNp63 is an ectodermal gatekeeper of epidermal morphogenesis

由 Shalom-Feuerstein, R, Lena, A M, Zhou, H, De La Forest Divonne, S, Van Bokhoven, H, Candi, E, Melino, G, Aberdam, D
出版 2011

Tooth agenesis and orofacial clefting: genetic brothers in arms?

由 Phan, M., Conte, F., Khandelwal, K. D., Ockeloen, C. W., Bartzela, T., Kleefstra, T., van Bokhoven, H., Rubini, M., Zhou, H., Carels, C. E. L.
發表在 Hum Genet (2016)

High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation

由 Veltman, J, Yntema, H, Lugtenberg, D, Arts, H, Briault, S, Huys, E, Osoegawa, K, de Jong, P, Brunner, H, v Geurts, van Bokhoven, H, Schoenmakers, E
出版 2004

Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10

由 van der Zwaag, B, Verzijl, H, d Beltran-Valero, Schuster, V, van Bokhoven, H, Kremer, H, van Reen, M, Wichers, G, Brunner, H, Padberg, G
出版 2002

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

由 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
出版 1998

A homozygous nonsense mutation in the Fukutin gene causes a Walker-Warburg syndrome phenotype

由 d Beltran-Valero, van Bokhoven, H, van Beusekom, E, Van den Akker, W, Kant, S, Dobyns, W, Cormand, B, Currier, S, Hamel, B, Talim, B, Topaloglu, H, Brunner, H
出版 2003

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker–Warburg syndrome

由 d Beltran-Valero, Voit, T, Longman, C, Steinbrecher, A, Straub, V, Yuva, Y, Herrmann, R, Sperner, J, Korenke, C, Diesen, C, Dobyns, W, Brunner, H, van Bokhoven, H, Brockington, M, Muntoni, F
出版 2004

Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation

由 Kleefstra, T, Yntema, H, Oudakker, A, Banning, M, Kalscheuer, V, Chelly, J, Moraine, C, Ropers, H, Fryns, J, Janssen, I, Sistermans, E, Nillesen, W, de Vries, L B A, Hamel, B, van Bokhoven, H
出版 2004

Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate

由 Laumonnier, F, Holbert, S, Ronce, N, Faravelli, F, Lenzner, S, Schwartz, C, Lespinasse, J, Van Esch, H, Lacombe, D, Goizet, C, Phan-Dinh, T, van Bokhoven, H, Fryns, J, Chelly, J, Ropers, H, Moraine, C, Hamel, B, Briault, S
出版 2005

Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.

由 van Bokhoven, H, Jung, M, Smits, A P, van Beersum, S, Rüschendorf, F, van Steensel, M, Veenstra, M, Tuerlings, J H, Mariman, E C, Brunner, H G, Wienker, T F, Reis, A, Ropers, H H, Hamel, B C
出版 1999

POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome

由 van Reeuwijk, J, Janssen, M, van den Elzen, C, d Beltran-Valero, Sabatelli, P, Merlini, L, Boon, M, Scheffer, H, Brockington, M, Muntoni, F, Huynen, M, Verrips, A, Walsh, C, Barth, P, Brunner, H, van Bokhoven, H
出版 2005

Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome

由 Kleefstra, T, Smidt, M, Banning, M, Oudakker, A, Van Esch, H, de Brouwer, A P M, Nillesen, W, Sistermans, E, Hamel, B, de Bruijn, D, Fryns, J, Yntema, H, Brunner, H, de Vries, B B A, van Bokhoven, H
出版 2005

Periventricular Heterotopia in Common Microdeletion Syndromes

由 van Kogelenberg, M., Ghedia, S., McGillivray, G., Bruno, D., Leventer, R., MacDermot, K., Nelson, J., Nagarajan, L., Veltman, J.A., de Brouwer, A.P., McKinlay Gardner, R.J., van Bokhoven, H., Kirk, E.P., Robertson, S.P.
出版 2010

Elevated microRNA-181c and microRNA-30d levels in the enlarged amygdala of the valproic acid rat model of autism

由 Olde Loohuis, N.F.M., Kole, K., Glennon, J.C., Karel, P., Van der Borg, G., Van Gemert, Y., Van den Bosch, D., Meinhardt, J., Kos, A., Shahabipour, F., Tiesinga, P., van Bokhoven, H., Martens, G.J.M., Kaplan, B.B., Homberg, J.R., Aschrafi, A.
發表在 Neurobiol Dis (2015)