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Disruption of twist1 translation by 5′ utr variants in saethre�chotzen syndrome

Zhou, Yan et al.

Human mutation. VOL 39; NUMBER 10, ; 2018, 1360-1365 -- John Wiley & Sons, Ltd

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Disruption of TWIST1 translation by 5′ UTR variants in Saethre‐Chotzen syndrome

Zhou, Yan et al.

Human mutation. Volume 39:Issue 10 (2018); pp 1360-1365 -- Wiley Blackwell

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Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12‐Related Craniosynostosis

Goos, Jacqueline A.C. et al.

Human mutation. Volume 37:Issue 8 (2016); pp 732-736 -- Wiley Blackwell

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