Are overweight and obese youths more often bullied by their peers? A meta-analysis on the relation between weight status and bullyingVAN GEEL, M; VEDDER, P; TANILON, J et al.International journal of obesity. 2014, Vol 38, Num 10, pp 1263-1267, issn 0307-0565, 5 p.Article

Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestryVAN TUYLL VAN SEROOSKERKEN, A. M; DRÖGEMÖLLER, B. I; TE VELDE, K et al.British journal of dermatology (1951). 2012, Vol 166, Num 2, pp 261-265, issn 0007-0963, 5 p.Article

The Missense Mutation G12D in Connexin30.3 Can Cause Both Erythrokeratodermia Variabilis of Mendes da Costa and Progressive Symmetric Erythrokeratodermia of GottronVAN STEENSEL, M. A. M; ORANJE, A. P; VAN DER SCHROEFF, J. G et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 4, pp 657-661, issn 1552-4825, 5 p.Article

A newly identified splice site mutation in ZMPSTE24 causes restrictive dermopathy in the Middle EastSANDER, C. S; SALMAN, N; VERSTRAETENT, V. L. R. M et al.British journal of dermatology (1951). 2008, Vol 159, Num 4, pp 961-967, issn 0007-0963, 7 p.Article

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsRIJKERS, T; DEIDDA, G; VAN DER MAAREL, S. M et al.Journal of medical genetics. 2004, Vol 41, Num 11, pp 826-836, issn 0022-2593, 11 p.Article

Molecular genetic support for the rule of dichotomy in type 2 segmental Darier diseaseFÖLSTER-HOLST, R; NELLEN, R. G. L; JENSEN, J.-M et al.British journal of dermatology (1951). 2012, Vol 166, Num 2, pp 464-466, issn 0007-0963, 3 p.Article

A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosisBOLLING, M. C; BLADERGROEN, R. S; VAN STEENSEL, M. A. M et al.British journal of dermatology (1951). 2010, Vol 162, Num 4, pp 875-879, issn 0007-0963, 5 p.Article

Defects in DNA mismatch repair do not account for early-onset basal cell carcinomaMOSTERD, K; NELLEN, R. G. L; VAN ENGELAND, M et al.British journal of dermatology (1951). 2008, Vol 159, Num 3, pp 751-753, issn 0007-0963, 3 p.Article

Clinically manifest X-linked recessive ichthyosis in a female due to a homozygous interstitial 1·6-Mb deletion of Xp22.31NAGTZAAM, I. F; STEGMANN, A. P. A; STEIJLEN, P. M et al.British journal of dermatology (1951). 2012, Vol 166, Num 4, pp 905-907, issn 0007-0963, 3 p.Article

Linkage refinement of Bazex―Dupré―Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1PARREN, L. J. M. T; ABUZAHRA, F; WAGENVOORT, T et al.British journal of dermatology (1951). 2011, Vol 165, Num 1, pp 201-203, issn 0007-0963, 3 p.Article

A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndromeDE ZWART-STORM, E. A; VAN GEEL, M; VEYSEY, E et al.British journal of dermatology (1951). 2011, Vol 164, Num 1, pp 197-199, issn 0007-0963, 3 p.Article

Lymphedema, cardiac septal defects, and characteristic facies : Possible new case of irons-bianchi syndromeVAN STEENSEL, M. A. M; VAN GEEL, M; SCHRANDER-STUMPEL, C et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 20, pp 2448-2451, issn 1552-4825, 4 p.Article

The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elementsVAN GEEL, M; HEATHER, L. J; LYLE, R et al.Genomics (San Diego, Calif.). 1999, Vol 61, Num 1, pp 55-65, issn 0888-7543Article

Wilms tumour as a possible early manifestation of hereditary leiomyomatosis and renal cell cancer?BADELOE, S; VAN SPAENDONCK-ZWARTS, K. Y; VAN STEENSEL, M. A. M et al.British journal of dermatology (1951). 2009, Vol 160, Num 3, pp 707-709, issn 0007-0963, 3 p.Article

Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702WVAN STEENSEL, M. A. M; BADELOE, S; WINNEPENNINCKX, V et al.Experimental dermatology. 2008, Vol 17, Num 12, pp 1057-1058, issn 0906-6705, 2 p.Article

Novel EBP gene mutations in Conradi-Hünermann-Happle syndromeSTEIJLEN, P. M; VAN GEEL, M; VREEBURG, M et al.British journal of dermatology (1951). 2007, Vol 157, Num 6, pp 1225-1229, issn 0007-0963, 5 p.Article

Further delineation of the hypotrichosis-deafness syndromeVAN STEENSEL, Maurice A. M; VAN GEEL, M; STEIJLEN, P. M et al.EJD. European journal of dermatology. 2005, Vol 15, Num 6, pp 437-438, issn 1167-1122, 2 p.Article

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35VAN DEUTEKOM, J. C. T; HOFKER, M. H; ROMBERG, S et al.Muscle & nerve. 1995, pp S19-S26, issn 0148-639X, SUP2Conference Paper

Phenotypic variability associated with WNT10A nonsense mutationsVAN GEEL, M; GATTAS, M; KESLER, Y et al.British journal of dermatology (1951). 2010, Vol 162, Num 6, pp 1403-1406, issn 0007-0963, 4 p.Article

A novel missense mutation in GJB2 disturbs gap junction protein transport and causes focal palmoplantar keratoderma with deafnessDE ZWART-STORM, E. A; HAMM, H; STOEVESANDT, J et al.Journal of medical genetics. 2008, Vol 45, Num 3, pp 161-166, issn 0022-2593, 6 p.Article

A modular, positive selection bacterial artificial chromosome vector with multiple cloning sitesFRENGEN, E; WEICHENHAN, D; BAOHUI ZHAO et al.Genomics (San Diego, Calif.). 1999, Vol 58, Num 3, pp 250-253, issn 0888-7543Article

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35VAN DEUTEKOM, J. C. T; LEMMERS, R. J. L. F; FRANTS, R. R et al.Human molecular genetics (Print). 1996, Vol 5, Num 5, pp 581-590, issn 0964-6906Article

Detection on a putative 30-kDa ligand of the cluster-2 antigenHELFRICH, W; VAN GEEL, M; THE, T. H et al.International journal of cancer. Supplement. 1994, Num 8, pp 70-75, issn 0898-6924Conference Paper

Environmental regulation of alcohol metabolism in thermotolerant methylotrophic bacillus strainsARFMAN, N; DE VRIES, K. J; MOZEZLAAR, H. R et al.Archives of microbiology. 1992, Vol 157, Num 3, pp 272-278, issn 0302-8933Article

Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 geneNELLEN, R. G. L; STEIJLEN, P. M; HENNIES, H. C et al.British journal of dermatology (1951). 2013, Vol 168, Num 6, pp 1372-1374, issn 0007-0963, 3 p.Article