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Article

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

Clinical dysmorphology - 1 Oct 2017

Bayat Allan, Kerr Bronwyn, Douzgou Sofia

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 28288023
DOI: 10.1097/MCD.0000000000000169

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