Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromesSTEIJLEN, P. M; VAN STEENSEL, M. A. M.American journal of medical genetics. 1999, Vol 85, Num 4, pp 359-360, issn 0148-7299Conference Paper

Internet databases for clinical geneticists : an overviewVAN STEENSEL, M. A. M; WINTER, R. M.Clinical genetics. 1998, Vol 53, Num 5, pp 323-330, issn 0009-9163Article

Genodermatoses caused by genetic mosaicismVREEBURG, M; VAN STEENSEL, M. A. M.European journal of pediatrics. 2012, Vol 171, Num 12, pp 1725-1735, issn 0340-6199, 11 p.Article

Gap junction diseases of the skinVAN STEENSEL, M. A. M.American journal of medical genetics. 2004, Vol 131C, Num 1, pp 12-19, issn 0148-7299, 8 p.Article

Genetics of psoriasisVAN STEENSEL, M. A. M; STEIJLEN, P. M.Clinics in dermatology. 1997, Vol 15, Num 5, pp 669-675, issn 0738-081XArticle

Clinical report. Two Dutch brothers with Borrone dermato-cardio-skeletal syndromeVAN STEENSEL, M. A. M; CEULEN, R. P. M; DELHAAS, T et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 11, pp 1223-1226, issn 1552-4825, 4 p.Article

New type of twin spotVAN STEENSEL, M. A. M; STEIJLEN, P. M; MAESSEN-VISCH, M. B et al.American journal of medical genetics. 2005, Vol 133A, Num 1, pp 108-111, issn 0148-7299, 4 p.Article

A new type of erythrokeratodermaVAN STEENSEL, M. A. M; VAN GEEL, M; STEIJLEN, P. M et al.British journal of dermatology (1951). 2005, Vol 152, Num 1, pp 155-158, issn 0007-0963, 4 p.Article

Genital porokeratosisLAINO, L; PALA, S; INNOCENZI, D et al.EJD. European journal of dermatology. 2004, Vol 14, Num 3, pp 190-192, issn 1167-1122, 3 p.Article

Clinical response to ustekinumab in familial pityriasis rubra pilaris caused by a novel mutation in CARD14EYTAN, O; SARIG, O; SPRECHER, E et al.British journal of dermatology (1951). 2014, Vol 171, Num 2, pp 420-422, issn 0007-0963, 3 p.Article

A Novel TP63 Mutation in Family With ADULT Syndrome Presenting With Eczema and HgpotheliaVAN ZELST-STAMS, W. A. G; VAN STEENSEL, M. A. M.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1558-1560, issn 1552-4825, 3 p.Article

Myhre syndrome in a female with previously undescribed symptoms : Further delineation of the phenotypeVAN STEENSEL, M. A. M; VREEBURG, M; STEIJLEN, P. M et al.American journal of medical genetics. 2005, Vol 139A, Num 2, pp 127-130, issn 0148-7299, 4 p.Article

A case of Rombo syndromeVAN STEENSEL, M. A. M; JASPERS, N. G. J; STEIJLEN, P. M et al.British journal of dermatology (1951). 2001, Vol 144, Num 6, pp 1215-1218, issn 0007-0963Article

Sweat testing in hypomelanosis of Ito : divergent results reflecting genetic heterogeneitySTEULEN, P. M; VIËTOR, H. E; VAN STEENSEL, M. A. M et al.EJD. European journal of dermatology. 2000, Vol 10, Num 3, pp 217-219, issn 1167-1122Article

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

Molecular aetiology and pathogenesis of basal cell carcinomaTILLI, C. M. L. J; VAN STEENSEL, M. A. M; KREKELS, G. A. M et al.British journal of dermatology (1951). 2005, Vol 152, Num 6, pp 1108-1124, issn 0007-0963, 17 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 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

Paraneoplastic hypertrichosis lanuginosa acquisita : uncommon or overlooked?SLEE, P. H. T. J; VAN DER WAAL, R. I. F; SCHAGEN VAN LEEUWEN, J. H et al.British journal of dermatology (1951). 2007, Vol 157, Num 6, pp 1087-1092, issn 0007-0963, 6 p.Article

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