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American Journal of Medical Genetics|June 28, 2001
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paragangliomaS Niemann, J Becker-Follmann, G Nürnberg, et al.
Acta Neurologica Scandinavica|March 3, 2001
Induction of sTNF-R1 and sTNF-R2 by interferon beta-1b in correlation with clinical and MRI activityC Laske, P Oschmann, J Tofighi, et al.
Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 15, 2021
Quality of life and clinical characteristics of self-improving congenital ichthyosis within the disease spectrum of autosomal-recessive congenital ichthyosisL Hake, K Süßmuth, K Komlosi, et al.
Annals of the Rheumatic Diseases|November 13, 2004
Lack of genetic association of the three more common polymorphisms of CARD15 with psoriatic arthritis and psoriasis in a German cohortJ Lascorz, H Burkhardt, U Hüffmeier, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 25, 2024
Personal, financial and time burden in inherited ichthyoses: A survey of 144 patients in a university-based settingC Klein, V Oji, R Sommer, et al.
The Journal of Investigative Dermatology|November 6, 1998
A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patientsB P Korge, E Healy, C S Munro, et al.
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