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	21.	Compound heterozygosity for ARS component B mutations in a Dutch patient with mal de Meleda. [electronic resource] by Nellen, R G L van Geel, M Steijlen, P M van Steensel, M A M Producer: 20090713 In: The British journal of dermatology vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Two Dutch brothers with Borrone dermato-cardio-skeletal syndrome. [electronic resource] by van Steensel, M A M Ceulen, R P M Delhaas, T de Die-Smulders, C Producer: 20070803 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Bile duct paucity is part of the neonatal ichthyosis-sclerosing cholangitis phenotype. [electronic resource] by Nagtzaam, I F van Geel, M Driessen, A Steijlen, P M van Steensel, M A M Producer: 20101222 In: The British journal of dermatology vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	A missense mutation in the type II hair keratin hHb3 is associated with monilethrix. [electronic resource] by van Steensel, M A M Steijlen, P M Bladergroen, R S Vermeer, M van Geel, M Producer: 20060331 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Homeostasis of the sebaceous gland and mechanisms of acne pathogenesis. [electronic resource] by Clayton, R W Göbel, K Niessen, C M Paus, R van Steensel, M A M Lim, X Producer: 20201221 In: The British journal of dermatology vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Defects in DNA mismatch repair do not account for early-onset basal cell carcinoma. [electronic resource] by Mosterd, K Nellen, R G L van Engeland, M van Geel, M van Steensel, M A M Producer: 20081222 In: The British journal of dermatology vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702W. [electronic resource] by van Steensel, M A M Badeloe, S Winnepenninckx, V Vreeburg, M Steijlen, P M van Geel, M Producer: 20090202 In: Experimental dermatology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	A case of Lelis syndrome with hystrix-like ichthyosis. [electronic resource] by van Steensel, M A M Winnepenninckx, V Nagtzaam, I F Janssens, R De Vos, R Steijlen, P M Producer: 20080903 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	The nuclear envelope, a key structure in cellular integrity and gene expression. [electronic resource] by Verstraeten, V L R M Broers, J L V Ramaekers, F C S van Steensel, M A M Producer: 20070628 In: Current medicinal chemistry vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. [electronic resource] by van Steensel, M A M Oranje, A P van der Schroeff, J G Wagner, A van Geel, M Producer: 20090617 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Focal dermal hypoplasia in a male patient due to mosaicism for a novel PORCN single nucleotide deletion. [electronic resource] by Vreeburg, M van Geel, M van den Heuij, L G T Steijlen, P M van Steensel, M A M Producer: 20110812 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Erysipelas as a sign of subclinical primary lymphoedema: a prospective quantitative scintigraphic study of 40 patients with unilateral erysipelas of the leg. [electronic resource] by Damstra, R J van Steensel, M A M Boomsma, J H B Nelemans, P Veraart, J C J M Producer: 20080820 In: The British journal of dermatology vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	[From gene to disease; cutaneous leiomyomatosis]. [electronic resource] by Badeloe, S van Geel, M van Steensel, M A M Steijlen, P M Poblete-Gutiérrez, P Frank, J A Producer: 20070322 In: Nederlands tijdschrift voor geneeskunde vol. 151 Availability: No items available. Save to lists Add to cart (remove)
	34.	A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosis. [electronic resource] by Bolling, M C Bladergroen, R S van Steensel, M A M Willemsen, M Jonkman, M F van Geel, M Producer: 20101006 In: The British journal of dermatology vol. 162 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Lymphedema, cardiac septal defects, and characteristic facies: possible new case of Irons-Bianchi syndrome. [electronic resource] by van Steensel, M A M van Geel, M Schrander-Stumpel, C Steijlen, P M Veraart, J C J M Producer: 20071206 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	HID and KID syndromes are associated with the same connexin 26 mutation. [electronic resource] by van Geel, M van Steensel, M A M Küster, W Hennies, H C Happle, R Steijlen, P M König, A Producer: 20020910 In: The British journal of dermatology vol. 146 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Darier disease: discrete phenotype in a Sinhalese patient with Darier disease. [electronic resource] by Nellen, R G L Arits, A H M M van Geel, M Steijlen, P M van Steensel, M A M Producer: 20160421 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Novel CLDN1 mutation in ichthyosis-hypotrichosis-sclerosing cholangitis syndrome without signs of liver disease. [electronic resource] by Nagtzaam, I F Peeters, V P M Vreeburg, M Wagner, A Steijlen, P M van Geel, M van Steensel, M A M Producer: 20190610 In: The British journal of dermatology vol. 178 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma. [electronic resource] by van Steensel, M A M Spruijt, L van der Burgt, I Bladergroen, R S Vermeer, M Steijlen, P M van Geel, M Producer: 20050418 In: American journal of medical genetics. Part A vol. 132A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Molecular aetiology and pathogenesis of basal cell carcinoma. [electronic resource] by Tilli, C M L J Van Steensel, M A M Krekels, G A M Neumann, H A M Ramaekers, F C S Producer: 20050804 In: The British journal of dermatology vol. 152 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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