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Dive into the research topics of 'Ulnar/fibular ray defect and brachydactyly in a family: A possible new autosomal dominant syndrome'. Together they form a unique fingerprint.- Sort by
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Éva Morava, Marta Czakó, Judit Kárteszi, Beatrix Cser, Karen Weissbecker, Karoly Méhes
Research output: Contribution to journal › Article › peer-review