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Dive into the research topics of 'Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects'. Together they form a unique fingerprint.- Sort by
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Amos J. Simon, Atar Lev, Yong Zhang, Batia Weiss, Anna Rylova, Eran Eyal, Nitzan Kol, Ortal Barel, Keren Cesarkas, Michalle Soudack, Noa Greenberg-Kushnir, Michele Rhodes, David L. Wiest, Ginette Schiby, Iris Barshack, Shulamit Katz, Elon Pras, Hana Poran, Haike Reznik-Wolf, Elena Ribakovsky
Research output: Contribution to journal › Article › peer-review