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American Journal of Medical Genetics|March 1, 1992
Psoriasis vulgaris, fetal growth, and genomic imprintingH Traupe, P J van Gurp, R Happle, et al.Acta Dermato-Venereologica|January 1, 1991
Epidermal transglutaminase in the ichthyosesC A van Hooijdonk, P M Steijlen, M Bergers, et al.Clinical Genetics|January 1, 1984
Ichthyosis vulgaris with hypogenitalism and hypogonadism: evidence for different genotypes by lipoprotein electrophoresis and steroid sulfatase testingH Traupe, C R Müller-Migl, G Kolde, et al.The Journal of Investigative Dermatology|April 1, 1990
Enzymatic distinction between two subgroups of autosomal recessive lamellar ichthyosisM Bergers, H Traupe, S C Dünnwald, et al.American Journal of Medical Genetics|July 9, 1999
Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred BlaschkoH TraupeEuropean Journal of Radiology|May 1, 1984
Relative cerebral perfusion by rapid sequence tomographyH TraupeDer Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 7, 2004
[Ichthyoses and related keratinization disorders. Management, clinical features and genetics]H TraupeJournal of the American Academy of Dermatology|September 1, 1991
How many epidermal nevus syndromes exist? A clinicogenetic classificationR HappleArchives of Dermatology|January 8, 1998
A rule concerning the segmental manifestation of autosomal dominant skin disorders. Review of clinical examples providing evidence for dichotomous types of severityR HappleDermatology (Basel, Switzerland)|January 1, 1997
Cancer proneness of linear porokeratosis may be explained by allelic lossR HapplePageof 38