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Dive into the research topics of 'Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly'. Together they form a unique fingerprint.- Sort by
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Lina Basel-Salmon, Noa Ruhrman-Shahar*, Ortal Barel, Ofir Hagari, Dina Marek-Yagel, Noy Azulai, Lily Bazak, Ran Svirsky, Haike Reznik-wolf, Gabriel Arie Lidzbarsky, Mordechai Shohat
Research output: Contribution to journal › Article › peer-review