Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency - Université de La Réunion Access content directly
Journal Articles Clinical Dysmorphology Year : 2010
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hal-01274630 , version 1 (16-02-2016)

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Jean-Luc Alessandri, Duksha Ramful, Fabrice Cuillier. Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency. Clinical Dysmorphology, 2010, 19 (2), pp.85--87. ⟨10.1097/MCD.0b013e328335c14a⟩. ⟨hal-01274630⟩
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