Search Results - Hotz, Alrun

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  1. 1
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    Autosomal dominant lamellar ichthyosis due to a missense variant in the gene NKPD1 by Komlosi, Katalin (Author) , Glocker, Cristina (Author) , Hsu-Rehder, Hao-Hsiang (Author) , Alter, Svenja (Author) , Kopp, Julia (Author) , Hotz, Alrun (Author) , Zimmer, Andreas David (Author) , Haußer-Siller, Ingrid (Author) , Sandhoff, Roger (Author) , Oji, Vinzenz (Author) , Fischer, Judith (Author) ,


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  2. 2
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    Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis by Hotz, Alrun Göntje (Author) , Haußer-Siller, Ingrid (Author) ,


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    Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis by Hotz, Alrun Göntje (Author) , Bourrat, Emmanuelle (Author) , Haußer-Siller, Ingrid (Author) ,


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  4. 4
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    Two novel mutations in the LOR gene in three families with loricrin keratoderma by Hotz, Alrun Göntje (Author) , Haußer-Siller, Ingrid (Author) ,


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