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European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 12, 2003
Clinical presentation of qualitative olfactory dysfunctionJ Frasnelli, B N Landis, S Heilmann, et al.The British Journal of Dermatology|May 25, 2013
Evidence for a polygenic contribution to androgenetic alopeciaS Heilmann, F F Brockschmidt, A M Hillmer, et al.Dermatology (Basel, Switzerland)|May 6, 1998
Conversion of psoriasis patients from the conventional formulation of cyclosporin A to a new microemulsion formulation: a randomized, open, multicentre assessment of safety and tolerabilityH Zachariae, B Abrams, S S Bleehen, et al.The Journal of Prevention of Alzheimer'S Disease|January 31, 2022
Association between 9p21-23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and DietN Mourtzi, A Hatzimanolis, G Xiromerisiou, et al.Clinical Genetics|September 20, 2017
Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palateA Mostowska, A Gaczkowska, K Żukowski, et al.Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.Journal of Dental Research|September 16, 2021
MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell MigrationL G Stüssel, R Hollstein, M Laugsch, et al.The British Journal of Dermatology|October 29, 2011
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldnessF F Brockschmidt, S Heilmann, J A Ellis, et al.European Psychiatry : the Journal of the Association of European Psychiatrists|June 18, 2016
Genome-wide association study of pathological gamblingM Lang, T Leménager, F Streit, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 30, 2024
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distalI Claus, S Sivalingam, A C Koller, et al.Pageof 20