Franz Rüschendorf
Max Delbrück Centrum für Molekulare Medizin Berlin Buch
8 papers found
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Front Cover, Volume 43, Issue 10
UploadRare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
UploadA biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
UploadGenetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
Download from doi.orgShared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
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