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Dive into the research topics of 'Wide phenotypic variations within a family with SALL1 mutations: Isolated external ear abnormalities to Goldenhar syndrome'. Together they form a unique fingerprint.- Sort by
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Rika Kosaki, Rika Fujimaru, Hazuki Samejima, Hiroshi Yamada, Kosuke Izumi, Kazumoto Iijima, Kenjiro Kosaki
Research output: Contribution to journal › Article › peer-review