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Dive into the research topics of 'Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: Implication for impaired sex development'. Together they form a unique fingerprint.- Sort by
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Goro Sasaki, Tsutomu Ogata, Tomohiro Ishii, Tomonobu Hasegawa, Seiji Sato, Nobutake Matsuo
Research output: Contribution to journal › Article › peer-review