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Dive into the research topics of 'Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip'. Together they form a unique fingerprint.- Sort by
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Eiki Yamachika, H. Tsujigiwa, Y. Ishiwari, N. Mizukawa, N. Nagai, T. Sugahara
Research output: Contribution to journal › Article › peer-review