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

Jean-Luc Alessandri 1, 2, 3 Duksha Ramful 2, 3 Fabrice Cuillier 2
1 Service de Réanimation Néonatale et Pédiatrique
2 CHU La Réunion - Centre Hospitalier Universitaire de La Réunion
3 GRI - Groupe de Recherche en Immunopathologies et maladies infectueuses
Abstract : no abstract
Keywords : Child Chondrodysplasia Punctata Female Hand Deformities Congenital Humans Infant Newborn Phenotype Pregnancy Pregnancy Complications Vitamin K Deficiency Young Adult
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https://hal.univ-reunion.fr/hal-01274630
Contributor : Réunion Univ <>
Submitted on : Tuesday, February 16, 2016 - 8:43:21 AM
Last modification on : Thursday, March 28, 2019 - 11:24:14 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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