Search Results - Fischer-Zirnsak, Björn

AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia by Terhal, Paulien (Author) , Venhuizen, Anton J. (Author) , Lessel, Davor (Author) , Tan, Wen-Hann (Author) , Alswaid, Abdulrahman (Author) , Grün, Regina (Author) , Alzaidan, Hamad I. (Author) , von Kroge, Simon (Author) , Ragab, Nada (Author) , Hempel, Maja (Author) , Kubisch, Christian (Author) , Novais, Eduardo (Author) , Cristobal, Alba (Author) , Tripolszki, Kornelia (Author) , Bauer, Peter (Author) , Fischer-Zirnsak, Björn (Author) , Nievelstein, Rutger A. J. (Author) , van Dijk, Atty (Author) , Nikkels, Peter (Author) , Oheim, Ralf (Author) , Hahn, Heidi (Author) , Bertoli-Avella, Aida (Author) , Maurice, Madelon M. (Author) , Kornak, Uwe (Author) ,

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SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy by Fischer-Zirnsak, Björn (Author) , Haußer-Siller, Ingrid (Author) , Thiel, Christian (Author) ,

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