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Clinical and Experimental Dermatology|January 9, 2010
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosisS Düzenli, S Redler, M Müller, et al.
Acta Dermato-Venereologica|April 13, 2005
KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutationAnette Bygum, Regina C Betz, Knud Kragballe, et al.
JID Innovations : Skin Science From Molecules to Population Health|June 24, 2026
Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disordersHadis Abdolahzadeh, Sabrina Henne, Amir Mokhlesi, et al.
Clinical and Experimental Dermatology|March 27, 2015
A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicismS Redler, S M Pasternack, S Wolf, et al.
Clinical and Experimental Dermatology|May 16, 2022
A new de novo heterozygous missense mutation in the desmoplakin gene, causing Naxos and Carvajal disease, associating oligodontia and nail fragilitySokounthie Ou, Nicole Cesarato, Pierre Mauran, et al.
European Journal of Dermatology : EJD|September 21, 2005
Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triadLaura Maintz, Regina C Betz, Jean-Pierre Allam, et al.
American Journal of Medical Genetics. Part A|September 4, 2010
Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutationAyse Tulin Mansur, Nursel H Elcioglu, Silke Redler, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1993
Characterization of four new gastric cancer cell linesH P Vollmers, K Stulle, J Dämmrich, et al.
Journal of Medical Genetics|July 31, 2012
Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literatureMatthias Begemann, Sabrina Spengler, Magdalena Gogiel, et al.
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