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JAMA Dermatology|September 12, 2014
The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndromeIris Spoerri, Michela Brena, Julie De Mesmaeker, et al.Clinical Implant Dentistry and Related Research|December 24, 2014
Lactotransferrin Gene (LTF) Polymorphisms and Dental Implant Loss: A Case-Control Association StudyAndrea Duarte Doetzer, Nina Schlipf, Fabiano Alvim-Pereira, et al.Neurogenetics|February 1, 2012
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, et al.Caries Research|May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries ExperienceAndrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.Acta Dermato-Venereologica|November 20, 2015
Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic IchthyosisAlrun Hotz, Vinzenz Oji, Emmanuelle Bourrat, et al.Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.Pageof 1