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Dive into the research topics of 'De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development'. Together they form a unique fingerprint.- Sort by
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Christopher T. Gordon, Shifeng Xue, Gökhan Yigit, Hicham Filali, Kelan Chen, Nadine Rosin, Koh Ichiro Yoshiura, Myriam Oufadem, Tamara J. Beck, Ruth McGowan, Alex C. Magee, Janine Altmüller, Camille Dion, Holger Thiele, Alexandra D. Gurzau, Peter Nürnberg, Dieter Meschede, Wolfgang Mühlbauer, Nobuhiko Okamoto, Vinod Varghese
Research output: Contribution to journal › Article › peer-review