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Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX).

AuthorsR Savarirayan
JournalPediatric radiology (Pediatr Radiol) Vol. 29 Issue 5 Pg. 322 (May 1999) ISSN: 0301-0449 [Print] Germany
PMID10382206 (Publication Type: Case Reports, Letter, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Anticoagulants
  • Warfarin
  • ARSL protein, human
  • Arylsulfatases
Topics
  • Anticoagulants (adverse effects)
  • Arylsulfatases (antagonists & inhibitors, genetics)
  • Chondrodysplasia Punctata (enzymology, etiology, genetics)
  • Female
  • Fetal Diseases (chemically induced, enzymology, genetics)
  • Genetic Linkage
  • Gestational Age
  • Humans
  • Infant, Newborn
  • Male
  • Maternal Exposure (adverse effects)
  • Mutation
  • Phenotype
  • Pregnancy
  • Warfarin (adverse effects)
  • X Chromosome

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