The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15

E Chabchoub, J R Vermeesch, T de Ravel, P de Cock, J-P Fryns

Research output: Contribution to journalArticlepeer-review

39 Citations (Scopus)
Original languageEnglish
Pages (from-to)189-92
Number of pages4
JournalJournal of Medical Genetics
Issue number3
Publication statusPublished - 2008


  • Adolescent
  • Chromosome Deletion
  • Chromosomes, Artificial, Bacterial/genetics
  • Chromosomes, Human, Pair 2/genetics
  • Craniofacial Abnormalities/genetics
  • Humans
  • Male
  • Phenotype
  • Protein-Serine-Threonine Kinases/genetics
  • Syndrome

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