Next Generation Sequencing of 8 gene panel: ALX3, ALX4, DHODH, EFNB1, EVC, EVC2, POLR1C, TCOF1.

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Ref: LV2236 Categories: , , , , , , , Diseases: Dysostoses with predominant craniofacial involvement: Frontonasal dysplasia, 1, 2. Miller syndrome (postaxial acrofacial dysostosis). Craniofrontonasal or Treacher Collins syGenes: ALX4, TCOF1, EVC, EFNB1-EN, DHODH, ALX3, POLR1C, EVC2Delivery term: 42 days