Andreas Janecke
Medical University of Innsbruck
111 papers found
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Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris
Download from www.nature.comGermlineLEMD3 mutations are rare in sporadic patients with isolated melorheostosis
Download from www.researchgate.netGJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Download from www.ncbi.nlm.nih.govEvidence for genetic heterogeneity in lymphedema-cholestasis syndrome
UploadThe canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis
UploadMolecular Genetics of Type 1 Glycogen Storage Disease
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