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

AuthorsJean-Luc Dominique Alessandri, Duksha Ramful, Fabrice Cuillier
JournalClinical dysmorphology (Clin Dysmorphol) Vol. 19 Issue 2 Pg. 85-87 (Apr 2010) ISSN: 1473-5717 [Electronic] England
PMID20177377 (Publication Type: Case Reports, Journal Article)
Topics
  • Child
  • Chondrodysplasia Punctata (complications)
  • Female
  • Hand Deformities, Congenital (complications, diagnostic imaging)
  • Humans
  • Infant
  • Infant, Newborn
  • Phenotype
  • Pregnancy
  • Pregnancy Complications (pathology)
  • Radiography
  • Vitamin K Deficiency (complications)
  • Young Adult

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