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Archives of Dermatology|March 23, 2005
Phacomatosis pigmentovascularis revisited and reclassifiedRudolf HappleDermatology (Basel, Switzerland)|February 9, 2002
Transposable elements and the lines of Blaschko: a new perspectiveRudolf HappleEuropean Journal of Dermatology : EJD|March 11, 2010
Type 2 segmental manifestation of "blue rubber bleb nevus syndrome": a reappraisal of 5 case reportsRudolf HappleActa Paediatrica (Oslo, Norway : 1992). Supplement|May 25, 2006
X-chromosome inactivation: role in skin disease expressionRudolf HappleJournal of the American Academy of Dermatology|November 22, 2008
What is a capillary malformation?Rudolf HappleAmerican Journal of Medical Genetics. Part A|October 24, 2015
The categories of cutaneous mosaicism: A proposed classificationRudolf HappleIndian Dermatology Online Journal|May 7, 2021
Progressive Osseous Heteroplasia is not an Autosomal Dominant Trait but Reflects Superimposed Mosaicism in Different GNAS Inactivation DisordersRudolf HappleAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 23, 2016
Goltz syndrome and PORCN: A view from EuropeRudolf HappleEuropean Journal of Medical Genetics|April 9, 2016
Progressive osseous heteroplasia is not a Mendelian trait but a type 2 segmental manifestation of GNAS inactivation disorders: A hypothesisRudolf HappleEuropean Journal of Dermatology : EJD|March 2, 2002
Speckled lentiginous nevus syndrome: delineation of a new distinct neurocutaneous phenotypeRudolf HapplePageof 23