2017
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Acanthosis nigricans in a Japanese boy with hypochondroplasia due to a K650T mutation in FGFR3
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Clinical Pediatric Endocrinology
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2016
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A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
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Clinical Pediatric Endocrinology
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1999
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Hypochondroplasia に黄色靱帯骨化症を合併し, 両下肢不全麻痺を呈した1例
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整形外科と災害外科
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1989
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当科における膝蓋骨脱臼の手術成績
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整形外科と災害外科
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1983
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胎児性軟骨異栄養症 (Hypochondroplasia) の1例
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日本口腔外科学会雑誌
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