Optimizing the growth of CoSi₂ film with oxide-mediated CoSi₂ template by silicon cap layerXU, M; VANTOMME, A; SMEETS, D et al.Journal of crystal growth. 2009, Vol 311, Num 16, pp 4007-4010, issn 0022-0248, 4 p.Article

Positional cloning of the gene for Nijmegen breakage syndromeMATSUURA, S; TAUCHI, H; OSHIMURA, M et al.Nature genetics. 1998, Vol 19, Num 2, pp 179-181, issn 1061-4036Article

A familial case of renal cell carcinoma and a t(2;3) chromosome translocationKOOLEN, M. I; VAN DER MEYDEN, A. P. M; BODMER, D et al.Kidney international. 1998, Vol 53, Num 2, pp 273-275, issn 0085-2538Article

Comparison of chromosome studies on PHA-stimulated blood and unstimulated bone marrow cells in recipients of lymphocyte depleted grafts using counterflow centrifugationSCHATTENBERG, A; BÄR, B; SMEETS, D et al.Bone marrow transplantation (Basingstoke). 1993, Vol 11, Num 2, pp 95-101, issn 0268-3369Article

Nijmegen breakage syndromeVAN DER BURGT, I; CHRZANOWSKA, K. H; SMEETS, D et al.Journal of medical genetics. 1996, Vol 33, Num 2, pp 153-156, issn 0022-2593Article

High prevalence of the Fra(X) syndrome cannot be explained by a high mutation rateSMITS, A; SMEETS, D; HAMEL, B et al.American journal of medical genetics. 1992, Vol 43, Num 1-2, pp 345-352, issn 0148-7299Article

Interphase cytogenetics of hematological cancer : comparison of classical karyotyping and in situ hybridization using a panel of eleven chromosome specific DNA probesPODDIGHE, P. J; MOESKER, O; SMEETS, D et al.Cancer research (Baltimore). 1991, Vol 51, Num 7, pp 1959-1967, issn 0008-5472, 9 p.Article

Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesVAN OOST, B. A; SMITS, A; DREESEN, J. C. F. M et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 328-331, issn 0148-7299Article

Genetic determination of fragile-site expressionSMEETS, D; ARETS, A.American journal of human genetics. 1990, Vol 47, Num 2, pp 196-201, issn 0002-9297, 6 p.Article

Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986―2007 in the NetherlandsDE GRAAF, G; HAVEMAN, M; HOCHSTENBACH, R et al.JIDR. Journal of intellectual disability research (Print). 2011, Vol 55, pp 462-473, issn 0964-2633, 12 p., 5Article

ICF syndrome : High variability of the chromosomal phenotype and association with classical hodgkin lymphomaSCHUETZ, C; BARBI, G; DEBATIN, K.-M et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 17, pp 2052-2057, issn 1552-4825, 6 p.Article

Assignment of the p150 subunit of the eukaryotic initiation factor 3A gene (EIF3A) to human chromosome band 10q26 by in situ hybridisationENSINGER, C; OBRIST, P; MIKUZ, G et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 74-75, issn 0301-0171Article

Another patient with a deletion 14qll.2q13GOVAERTS, L; TOORMAN, J; BLIJ-PHILIPSEN, M. V. D et al.Annales de génétique (Paris). 1996, Vol 39, Num 4, pp 197-200, issn 0003-3995Article

Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosomeHULSEBOS, T; WIERINGA, B; HOCHSTENBACH, R et al.Cytogenetics and cell genetics. 1986, Vol 43, Num 1-2, pp 47-56, issn 0301-0171Article

On the thermal expansion coefficient of CoSi₂ and NiSi₂SMEETS, D; VANHOYLAND, G; D'HAEN, J et al.Journal of physics. D, Applied physics (Print). 2009, Vol 42, Num 23, issn 0022-3727, 235402.1-235402.7Article

Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDDE GREEF, J. C; WOHLGEMUTH, M; CHAN, O. A et al.Neurology. 2007, Vol 69, Num 10, pp 1018-1026, issn 0028-3878, 9 p.Article

Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA)KOOLEN, D. A; NILLESEN, W. M; SMEETS, D et al.Journal of medical genetics. 2004, Vol 41, Num 12, pp 892-899, issn 0022-2593, 8 p.Article

At least nine cases of trisomy 11q23→qter in one generation as a result of familial t(11;13) translocationSMEETS, D; VAN RAVENSWAAIJ, C; DE PATER, J et al.Journal of medical genetics. 1997, Vol 34, Num 1, pp 18-23, issn 0022-2593Article

Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24MATSUURA, S; WEEMAES, C; OSHIMURA, M et al.American journal of human genetics. 1997, Vol 60, Num 6, pp 1487-1494, issn 0002-9297Article

No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesJANSEN, G; BARTOLOMEI, M; KALSCHEUER, V et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, pp 1221-1227, issn 0964-6906Article

Mixed hematopoietic chimerism after allogeneic transplantation with lymphocyte-depleted bone marrow is not associated with a higher incidence of relapseSCHATTENBERG, A; DE WITTE, T; SALDEN, M et al.Blood. 1989, Vol 73, Num 5, pp 1367-1372, issn 0006-4971Article

Plasma circulating tumor DNA as an alternative to metastatic biopsies for mutational analysis in breast cancerROTHE, F; LAES, J.-F; DETIFFE, J.-P et al.Annals of oncology. 2014, Vol 25, Num 10, pp 1959-1965, issn 0923-7534, 7 p.Article

Determination of the dominant diffusing species during nickel and palladium germanide formationCOMRIE, C. M; SMEETS, D; PONDO, K. J et al.Thin solid films. 2012, Vol 526, pp 261-268, issn 0040-6090, 8 p.Article

Fabrication, characterization and modeling of single-crystal thin film calorimeter sensorsANAHORY, Y; GUIHARD, M; RODRIGUEZ-VIEJO, J et al.Thermochimica acta. 2010, Vol 510, Num 1-2, pp 126-136, issn 0040-6031, 11 p.Article

Dependence of the sticking coefficient of sputtered atoms on the target-substrate distanceMAHIEU, S; VAN AEKEN, K; DEPLA, D et al.Journal of physics. D, Applied physics (Print). 2008, Vol 41, Num 15, issn 0022-3727, 152005.1-152005.4Article