The p63 gene in EEC and other syndromes

द्वारा Brunner, H, Hamel, B, van Bokhoven, H
प्रकाशित 2002

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

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

MicroRNA networks direct neuronal development and plasticity

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

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

द्वारा Kroeze, Y, Peeters, D, Boulle, F, van den Hove, D L A, van Bokhoven, H, Zhou, H, Homberg, J R
में प्रकाशित Transl Psychiatry (2016)

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

द्वारा Kroeze, Y, Peeters, D, Boulle, F, van den Hove, D L A, van Bokhoven, H, Zhou, H, Homberg, J R
में प्रकाशित 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

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

ΔNp63 is an ectodermal gatekeeper of epidermal morphogenesis

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

Tooth agenesis and orofacial clefting: genetic brothers in arms?

द्वारा 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.
में प्रकाशित Hum Genet (2016)

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

द्वारा 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
प्रकाशित 2004

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

द्वारा 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
प्रकाशित 2002

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

द्वारा 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
प्रकाशित 1998

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

द्वारा 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
प्रकाशित 2003

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

द्वारा 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
प्रकाशित 2004

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

द्वारा 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
प्रकाशित 2004

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

द्वारा 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
प्रकाशित 2005

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

द्वारा 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
प्रकाशित 1999

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

द्वारा 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
प्रकाशित 2005

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

द्वारा 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
प्रकाशित 2005

Periventricular Heterotopia in Common Microdeletion Syndromes

द्वारा 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.
प्रकाशित 2010

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

द्वारा 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.
में प्रकाशित Neurobiol Dis (2015)