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Current Osteoporosis Reports|June 22, 2010
Assessment of individual fracture risk: FRAX and beyondJoop P W van den Bergh, Tineke A C M van Geel, Willem F Lems, et al.
American Journal of Medical Genetics. Part A|March 18, 2009
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of GottronM A M van Steensel, A P Oranje, J G van der Schroeff, et al.
Maturitas|January 8, 2010
Individualizing fracture risk predictionTineke A C M van Geel, Joop P W van den Bergh, Geert-Jan Dinant, 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.
Current Osteoporosis Reports|November 30, 2010
Optimal use of vitamin D when treating osteoporosisJoop P W van den Bergh, Sandrine P G Bours, Tineke A C M van Geel, et al.
The British Journal of Dermatology|May 27, 2010
A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosisM C Bolling, R S Bladergroen, M A M van Steensel, 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.
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