A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP)

Liesbeth Spruijt, Pieter Verdyck, Wim Van Hul, Wim Wuyts, Christine de Die-Smulders

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)
Original languageEnglish
Pages (from-to)45-47
Number of pages3
JournalAmerican Journal of Medical Genetics. Part A
Volume139
Issue number1
DOIs
Publication statusPublished - 15 Nov 2005

Keywords

  • DNA-Binding Proteins/genetics
  • Female
  • Homeodomain Proteins/genetics
  • Humans
  • Infant
  • Infant, Newborn
  • Mutation
  • Parietal Bone/abnormalities
  • Radiography
  • Transcription Factors/genetics

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