The evolving craniofacial phenotype of a patient with Sensenbrenner syndrome caused by IFT140 compound heterozygous mutations

Clin Dysmorphol. 2017 Mar 10.DOI:10.1097/MCD.0000000000000169 [Epub ahead of print]

Bayat A, Kerr B, Douzgou S; DDD Study

https://www.ncbi.nlm.nih.gov/pubmed/28288023

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