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

Jean-Luc Alessandri; Duksha Ramful; Fabrice Cuillier

doi:10.1097/MCD.0b013e328335c14a

Journal articles

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

Document type :

Journal articles

Domain :

Life Sciences [q-bio]

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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, July 1, 2021 - 3:06:24 AM

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

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

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