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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 7, 2004
Molecular genetics of hereditary hair and nail diseaseM A M van Steensel, M van Geel, P M SteijlenThe British Journal of Dermatology|September 5, 2002
New syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin CM A M Van Steensel, M Van Geel, P M SteijlenThe British Journal of Dermatology|January 20, 2005
A new type of erythrokeratodermaM A M van Steensel, M van Geel, P M SteijlenThe British Journal of Dermatology|July 22, 2010
Bile duct paucity is part of the neonatal ichthyosis-sclerosing cholangitis phenotypeI F Nagtzaam, M van Geel, A Driessen, et al.Experimental Dermatology|July 12, 2008
Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702WM A M van Steensel, S Badeloe, V Winnepenninckx, et al.Nederlands Tijdschrift Voor Geneeskunde|March 1, 2007
[From gene to disease; cutaneous leiomyomatosis]S Badeloe, M van Geel, M A M van Steensel, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|July 15, 2010
Focal dermal hypoplasia in a male patient due to mosaicism for a novel PORCN single nucleotide deletionM Vreeburg, M van Geel, L G T van den Heuij, et al.American Journal of Medical Genetics. Part A|September 14, 2007
Lymphedema, cardiac septal defects, and characteristic facies: possible new case of Irons-Bianchi syndromeM A M van Steensel, M van Geel, C Schrander-Stumpel, et al.The British Journal of Dermatology|June 20, 2002
HID and KID syndromes are associated with the same connexin 26 mutationM van Geel, M A M van Steensel, W Küster, et al.American Journal of Medical Genetics. Part A|November 20, 2004
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratodermaM A M van Steensel, L Spruijt, I van der Burgt, et al.Pageof 25