Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency - Université de La Réunion
Journal Articles Clinical Dysmorphology Year : 2010

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

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Life Sciences [q-bio]

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https://hal.univ-reunion.fr/hal-01274630

Submitted on : Tuesday, February 16, 2016-8:43:21 AM

Last modification on : Monday, March 20, 2023-7:48:08 AM

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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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