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Craniometaphyseal dysplasia and chondrocalcinosis cosegregating in a family with an ANKH mutation.

AuthorsGareth Baynam, Jack Goldblatt, Lyn Schofield
JournalAmerican journal of medical genetics. Part A (Am J Med Genet A) Vol. 149A Issue 6 Pg. 1331-3 (Jun 2009) ISSN: 1552-4833 [Electronic] United States
PMID19449425 (Publication Type: Journal Article)
Chemical References
  • ANKH protein, human
  • Phosphate Transport Proteins
Topics
  • Adult
  • Chondrocalcinosis (diagnostic imaging, genetics)
  • Family
  • Humans
  • Infant
  • Male
  • Mutation
  • Phosphate Transport Proteins (genetics)
  • Radiography

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