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Browsing by Faculty / Department Human Genetics

Full Text	Issue Date	Title	Author(s)
	1993	Detection of Mycoplasma pulmonis in experimentally infected laboratory rats by 16S rRNA amplification.	Kuppeveld, F.J.M. van; Melchers, W.J.G.; Willemse, H.F.; Kissing, J.; Galama, J.M.D., et al
	1994	16S rRNA based polymerase chain reaction compared with culture and serological methods for diagnosis of Mycoplasma pneumoniae infection.	Kuppeveld, F.J.M. van; Johansson, K.E.; Galama, J.M.D.; Kissing, J.; Bolske, G., et al
	1994	Detection of mycoplasma contamination in cell cultures by a mycoplasma group-specific PCR.	Kuppeveld, F.J.M. van; Johansson, K.E.; Galama, J.M.D.; Kissing, J.; Bolske, G., et al
	1994	No evidence of mycoplasmas in peripheral blood mononuclear cell fraction of HIV-infected patients.	Kuppeveld, F.J.M. van; Melchers, W.; Kissing, J.; Logt, J. van der; Galama, J.
	1998	Evaluation of speech synthesis systems for Dutch in telecommunications applications	Sluijter, A.M.C.; Bosgoed, E.A.J.; Kerkhoff, J.J.P.; Meier, E.; Rietveld, T., et al
	2003	Approximate inference and constrained optimization	Heskes, T.; Albers, C.A.; Kappen, H.J.
	2003	Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis.	Willemsen, R.; Smits, A.P.T.; Severijnen, L.A.; Jansen, M.; Jacobs, A.J.M, et al
	2004	A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridization.	Koolen, D.A.; Vissers, L.E.L.M.; Nillesen, W.M.; Smeets, D.F.C.M.; Ravenswaaij-Arts, C.M.A. van, et al
	2004	Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy.	Seynaeve, C.; Verhoog, L.C.; Bosch, L.M. van de; Geel, A.N. van; Menke-Pluymers, M., et al
	2004	Three new families with arterial tortuosity syndrome.	Wessels, M.W.; Catsman-Berrevoets, C.E.; Mancini, G.M.; Breuning, M.H.; Hoogeboom, J.J., et al
	2004	Intratumoral administration of recombinant human interleukin 12 in head and neck squamous cell carcinoma patients elicits a T-helper 1 profile in the locoregional lymph nodes.	Herpen, C.M.L. van; Looman, M.W.G.; Zonneveld-Vrieling, M.N.; Scharenborg, N.M.; Wilde, P.C.M. de, et al
	2004	High prevalence of SLC6A8 deficiency in X-linked mental retardation.	Rosenberg, E.H.; Almeida, L.S.; Kleefstra, T.; Grauw, R.S. de; Yntema, H.G., et al
	2004	Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12).	Pennings, R.J.E.; Topsakal, V.; Astuto, L.M.; Brouwer, A.P.M. de; Wagenaar, M., et al
	2004	Hydrops foetalis als mogelijk gevolg van erfelijke stofwisselingsziekten	Janssens, P.M.W.; Jong, J.G.N. de; Liebrand-van Sambeek, M.L.F.; Wevers, R.A.; Groot, A. de, et al
	2004	Phenotypic characteristics of male subfertility and its familial occurrence.	Golde, R.J.T. van; Avoort, I.A.M. van der; Tuerlings, J.H.A.M.; Kiemeney, L.A.L.M.; Meuleman, E.J.H., et al
	2004	Autosomal dominant rhegmatogenous retinal detachment--clinical appearance and surgical outcome.	Theelen, T.; Go, S.L.; Tilanus, M.A.D.; Klevering, B.J.; Deutman, A.F., et al
	2004	Attitudes of potential providers toward preconceptual cystic fibrosis carrier screening.	Poppelaars, F.; Ader, H.J.; Cornel, M.C.; Henneman, L.; Hermens, R.P.M.G., et al
	2004	A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutation.	Steensel, M.A.M. van; Steijlen, P.M.; Bladergroen, R.; Hoefsloot, L.H.; Ravenswaaij-Arts, C.M.A. van, et al
	2004	Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II.	Wijk, E. van; Pennings, R.J.E.; Brinke, H. te; Claassen, A.M.W.; Yntema, H.G., et al
	2004	Chromosome 3 translocations and familial renal cell cancer.	Bonne, A.; Bodmer, D.; Schoenmakers, E.F.P.M.; Ravenswaaij-Arts, C.M.A. van; Hoogerbrugge-van der Linden, N., et al