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Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency

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https://hal.univ-reunion.fr/hal-01274630
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Submitted on : Tuesday, February 16, 2016 - 8:43:21 AM
Last modification on : Friday, February 25, 2022 - 3:19:38 AM

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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, Lippincott, Williams & Wilkins, 2010, 19 (2), pp.85--87. ⟨10.1097/MCD.0b013e328335c14a⟩. ⟨hal-01274630⟩

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