Microdeletion of the FBXO11-gene and the MSH6-gene at 2p16.3 is likely to cause a distinct microcephaly, mental retardation, facial dysmorphism syndrome associated with an increased risk for intestinal cancer.

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• Microdeletion of the FBXO11-gene and the MSH6-gene at 2p16.3 is likely to cause a distinct microcephaly, mental retardation, facial dysmorphism syndrome associated with an increased risk for intestinal cancer.

  Publikation: Beitrag in Fachzeitschrift › Konferenzabstract