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European Journal of Endocrinology|October 20, 1999
Neonatal diabetes mellitus with hypergalactosemiaH Kentrup, J Altmüller, R Pfäffle, et al.
American Journal of Human Genetics|September 21, 2001
Genomewide scans of complex human diseases: true linkage is hard to findJ Altmüller, L J Palmer, G Fischer, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 15, 2004
Asthma is associated with single-nucleotide polymorphisms in ADAM33M Werner, N Herbon, H Gohlke, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 25, 2005
Single nucleotide polymorphism screening and association analysis--exclusion of integrin beta 7 and vitamin D receptor (chromosome 12q) as candidate genes for asthmaC Vollmert, T Illig, J Altmüller, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 15, 2015
Clinical and genetic findings in a family with NMNAT1-associated Leber congenital amaurosis: case report and review of the literatureA Hedergott, A E Volk, P Herkenrath, et al.
Journal of Molecular and Cellular Cardiology|July 6, 2017
Identification of circular RNAs with host gene-independent expression in human model systems for cardiac differentiation and diseaseD Siede, K Rapti, A A Gorska, et al.
Clinical Genetics|December 23, 2016
Genetic heterogeneity in Pakistani microcephaly families revisitedI Ahmad, S M Baig, A R Abdulkareem, et al.
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